Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome 7:128240525 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10368656

HGVS name

7:g.128240525C>G

About this variant

This variant overlaps 1 transcript and has 2774 individual genotypes.

Variation displays