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rs137852225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852225(A;A)
Make rs137852225(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537138
GeneF9
is asnp
is mentioned by
dbSNPrs137852225
ebirs137852225
HLIrs137852225
Exacrs137852225
Varsomers137852225
Maprs137852225
PheGenIrs137852225
hapmaprs137852225
1000 genomesrs137852225
hgdprs137852225
ensemblrs137852225
gopubmedrs137852225
geneviewrs137852225
scholarrs137852225
googlers137852225
pharmgkbrs137852225
gwascentralrs137852225
openSNPrs137852225
23andMers137852225
23andMe allrs137852225
SNP Nexus

SNPshotrs137852225
SNPdbers137852225
MSV3drs137852225
GWAS Ctlgrs137852225
Max Magnitude0
OMIM300746
Desc
Variant0013
Relatedalso
ClinVar
Risk rs137852225(A;A)
Alt rs137852225(A;A)
Reference rs137852225(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene F9
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000023.11:g.139537138G>A
CLNSRC ClinVar
CLNACC RCV000073092.2,