Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.08 (G)
Location

Chromosome 10:31429519 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs172849, rs56692821

HGVS names

This variant has 25 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2508 sample genotypes.

Variant displays