Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 9:37429981 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB NM_012203.1:c.598+145G>T

This variation has 10 HGVS names - click the plus to show

Variation displays