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rs137852841

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852841(C;T)
Make rs137852841(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position45064493
GeneCCM2
is asnp
is mentioned by
dbSNPrs137852841
ebirs137852841
HLIrs137852841
Exacrs137852841
Varsomers137852841
Maprs137852841
PheGenIrs137852841
hapmaprs137852841
1000 genomesrs137852841
hgdprs137852841
ensemblrs137852841
gopubmedrs137852841
geneviewrs137852841
scholarrs137852841
googlers137852841
pharmgkbrs137852841
gwascentralrs137852841
openSNPrs137852841
23andMers137852841
23andMe allrs137852841
SNP Nexus

SNPshotrs137852841
SNPdbers137852841
MSV3drs137852841
GWAS Ctlgrs137852841
Max Magnitude0
OMIM607929
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852841(T;T)
Alt rs137852841(T;T)
Reference rs137852841(C;C)
Significance Pathogenic
Disease Cerebral cavernous malformations 2
Variation info
Gene CCM2
CLNDBN Cerebral cavernous malformations 2
Reversed 0
HGVS NC_000007.13:g.45104092C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002800.2,