Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (G)

Chromosome 19:51888735 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17835331, rs57978823

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2579 sample genotypes.

Variant displays