Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 11:31515035 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs10835779, rs58102465

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays