Original source

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

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

Chromosome 12:12715767 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs117750150

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2507 sample genotypes and is mentioned in 1 citation.

Variant displays