Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 9:114804160 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

9:g.114804160A>G
ENST00000374045.4:c.210+1643T>C

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

Variation displays