Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.29 (T)
Location

Chromosome 8:39916080 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61687662

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2511 sample genotypes.

Variant displays