Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.20 (T)
Location

Chromosome 1:197325908 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

1:g.197325908T>G
ENST00000538660.1:c.989-53T>G
ENST00000367399.2:c.653-53T>G
ENST00000484075.1:c.989-53T>G
ENST00000535699.1:c.782-53T>G
ENST00000543483.1:c.86-53T>G
ENST00000475659.1:n.1126-53T>G
ENST00000367400.3:c.989-53T>G

This variation has assays on 9 chips - click the plus to show

Variation displays