Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)

Chromosome 1:230716578 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs113065244, rs59073550

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2529 sample genotypes.

Variant displays