Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.43 (T)
Location

Chromosome 15:88855879 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs71408892, rs71408893

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2508 sample genotypes.

Variant displays