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rs16969968 variant

Aliases
Asp398Asn, CHRNA5 (Ex5-54, D398N), CHRNA5 SNP rs16969968, CHRNA5 rs16969968, CHRNA5-rs16969968, D398N, Rs16969968, asparagine allele at CHRNA5 rs16969968, non-synonymous SNP in CHRNA5, non-synonymous coding SNP rs16969968, risk polymorphism rs16969968, rs16969968, rs16969968-A allele, rs16969968-AA genotype, rs16969968:G>A, rs16969968[N]
External links
dbSNP · ClinVar
Evidence from: primary | all sources

Related entities (9)

SubjectRelationObjectp-valueEvidence
rs16969968 associated_with CHRNA5 9
rs16969968 associated_with CHRNA5-CHRNA3-CHRNB4 cluster 0 1
rs16969968 associated_with cigarettes 3
rs16969968 risk_factor_for cigarettes 0 2
rs16969968 risk_factor_for nicotine 8
rs16969968 risk_factor_for smoking quantity 2
rs16969968 risk_factor_for tobacco use 1
rs16969968 interacts_with trauma exposure 1
trauma exposure interacts_with rs16969968 1

Mentioned in (3)

Papers in which this entity is mentioned.

Merged raw entities (15)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.

Raw name Type Papers Mentions
rs16969968 variant 22 110
d398n variant 1 1
rs16969968:g>a variant 1 2
asp398asn variant
asparagine allele at chrna5 rs16969968 variant
chrna5 (ex5-54, d398n) variant
chrna5 rs16969968 variant
chrna5-rs16969968 variant
chrna5 snp rs16969968 variant
non-synonymous coding snp rs16969968 variant
non-synonymous snp in chrna5 variant
risk polymorphism rs16969968 variant
rs16969968-aa genotype variant
rs16969968-a allele variant
rs16969968[n] variant