Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 22 sample genotypes.

Variant displays