Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 7 HGVS names - click the plus to show

17:g.3939197G>A
ENST00000359983.7:c.2101-1561C>T
ENST00000397043.7: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

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 3966 sample genotypes.

Variant displays