Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.34 (C)
Location

Chromosome 14:35401248 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386580201, rs57862712

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 11 transcripts, has 4063 sample genotypes and is mentioned in 4 citations.

Variant displays