Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.01 (G)
Location

Chromosome 14:102080475 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59380420, rs34399705

HGVS name

14:g.102080475C>G

About this variant

This variant overlaps 8 transcripts and has 2709 sample genotypes.

Variant displays