Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 15:88855708 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs11633195

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2505 sample genotypes.

Variant displays