Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.04 (C)
Location

Chromosome 1:231363683 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

1:g.231363683G>C

About this variant

This variant overlaps 2 transcripts and has 2505 sample genotypes.

Variant displays