Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.08 (A)
Location

Chromosome 17:4903133 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs116968995

HGVS name

17:g.4903133G>A

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays