Original source

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

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

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
ENST00000532708.5:n.96-199T>C
ENST00000340026.10:c.-92-211T>C

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2508 sample genotypes and is mentioned in 5 citations.

Variant displays