Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.30 (T)
Location

Chromosome 10:49608897 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60083637

HGVS name

10:g.49608897C>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3692 sample genotypes and is mentioned in 5 citations.

Variant displays