Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 15:90810242 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1269993

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 22 sample genotypes.

Variant displays