Original source

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

Alleles
T/-|Ancestral: T
Location

Chromosome 11:102599030 (forward strand)|View in location tab

Co-located variant

dbSNP rs372588239 (T/G)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61110135, rs151047297

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays