Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.06 (C)
Location

Chromosome 14:102080627 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60650263

HGVS name

14:g.102080627C>T

About this variant

This variant overlaps 8 transcripts and has 2512 sample genotypes.

Variant displays