Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.17 (A)
Location

Chromosome 17:3939197 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Hide

17:g.3939197G>A
ENST00000397043.7:c.2101-1561C>T
ENST00000359983.7:c.2101-1561C>T
ENST00000309890.11:c.2101-1561C>T
ENST00000397035.7:c.2101-1561C>T
ENST00000397041.7:c.2101-1561C>T
ENST00000352011.7:c.2101-1561C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 9 transcripts and has 3966 sample genotypes.

Variant displays