Original source

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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2798 sample genotypes and is mentioned in 5 citations.

Variant displays