Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 6:111922720 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

6:g.111922720A>G
ENST00000368761.5:c.-9+4259T>C
ENST00000392556.4:c.-1355-211T>C
ENST00000359831.4:c.-9+4259T>C
ENST00000528599.1:n.187+4259T>C
ENST00000531702.1:n.1643A>G
ENST00000340026.6:c.-92-211T>C
ENST00000532708.1:n.96-199T>C

This variation has assays on 6 chips - click the plus to show

Variation displays