Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.04 (T)
Location

Chromosome 14:102080300 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60287289, rs34002917

HGVS name

14:g.102080300C>T

About this variant

This variant overlaps 8 transcripts and has 2694 sample genotypes.

Variant displays