Original source

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

Alleles
T/C/G | Ancestral: T | Ambiguity code: B
Location

Chromosome 9:37436760 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002279

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variation displays