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rs137853140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853140(C;G)
Make rs137853140(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position92235531
GeneKRIT1
is asnp
is mentioned by
dbSNPrs137853140
ebirs137853140
HLIrs137853140
Exacrs137853140
Varsomers137853140
Maprs137853140
PheGenIrs137853140
hapmaprs137853140
1000 genomesrs137853140
hgdprs137853140
ensemblrs137853140
gopubmedrs137853140
geneviewrs137853140
scholarrs137853140
googlers137853140
pharmgkbrs137853140
gwascentralrs137853140
openSNPrs137853140
23andMers137853140
23andMe allrs137853140
SNP Nexus

SNPshotrs137853140
SNPdbers137853140
MSV3drs137853140
GWAS Ctlgrs137853140
Max Magnitude0
OMIM604214
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137853140(G;G)
Alt rs137853140(G;G)
Reference rs137853140(C;C)
Significance Pathogenic
Disease Cerebral cavernous malformations 1
Variation info
Gene KRIT1
CLNDBN Cerebral cavernous malformations 1
Reversed 1
HGVS NC_000007.13:g.91864845G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006080.2,