Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.01 (G)

Chromosome 6:128881679 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs68101737

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2506 sample genotypes.

Variant displays