Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.18 (C)
Location

Chromosome 15:74030090 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61059492

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 2507 sample genotypes.

Variant displays