Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.22 (A)

Chromosome 5:149899007 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56809693, rs414295

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 3050 sample genotypes.

Variant displays