Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.06 (A)
Location

Chromosome 7:128241090 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs10344223

HGVS name

7:g.128241090C>A

About this variant

This variant overlaps 1 transcript, has 2669 sample genotypes and is mentioned in 4 citations.

Variant displays