Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.18 (C)

Chromosome 1:20650019 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs57064662, rs3738137

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2579 sample genotypes.

Variant displays