Original source

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

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

Chromosome 9:104885374 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60254778

This variation has 4 HGVS names - click the plus to show

9:g.104885374G>A
ENST00000374733.1:c.-20-806C>T
ENST00000374736.5:c.161-806C>T
ENST00000423487.4:c.161-806C>T

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

Variation displays