Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 9:136500515 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR014914

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60944937

HGVS name

9:g.136500515T>C

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays