Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)
Location

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

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

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

6:g.111601517A>G
ENST00000531702.1:n.1643A>G
ENST00000368761.7:c.-9+4259T>C
ENST00000359831.6:c.-9+4259T>C
ENST00000528599.1:n.187+4259T>C
ENST00000532708.3:n.96-199T>C
ENST00000340026.8:c.-92-211T>C

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

Variation displays