Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.31 (T)
Location

Chromosome 9:114790605 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59393366

This variation has 3 HGVS names - click the plus to show

9:g.114790605T>C
ENST00000374044.1:c.372A>G
ENST00000374045.4:c.603A>G

This variation has assays on 8 chips - click the plus to show

Variation displays