Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)

Chromosome 7:99906002 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs10342838

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays