Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.09 (C)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs68101737

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2506 individual genotypes.

Variation displays