Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.07 (C)
Location

Chromosome 10:111075351 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57125560, rs17186373

HGVS name

10:g.111075351A>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 3896 sample genotypes and is mentioned in 1 citation.

Variant displays