Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 9:27548323 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs12237109, rs1300547

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

About this variant

This variant overlaps 4 transcripts and has 271 individual genotypes.

Variation displays