Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.11 (G)
Location

Chromosome 6:111601517 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 7 HGVS names - Hide

6:g.111601517A>G
ENST00000531702.1:n.1643A>G
ENST00000368761.9:c.-9+4259T>C
ENST00000359831.8:c.-9+4259T>C
ENST00000528599.1:n.187+4259T>C
ENST00000340026.10:c.-92-211T>C
ENST00000532708.5:n.96-199T>C

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3692 sample genotypes and is mentioned in 5 citations.

Variant displays