Original source

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

G/A|Ancestral: A|Ambiguity code: R|MAF: 0.43 (G)

Chromosome 19:41349610 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2558 sample genotypes and is mentioned in 2 citations.

Variant displays