Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.49 (T)
Location

Chromosome 11:108329415 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs641315

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2508 sample genotypes.

Variant displays