Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.39 (A)

Chromosome 1:115287322 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3729540

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanHap650Y, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 4077 sample genotypes.

Variant displays