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rs267607204

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607204(A;A)
Make rs267607204(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position92234451
GeneKRIT1
is asnp
is mentioned by
dbSNPrs267607204
ebirs267607204
HLIrs267607204
Exacrs267607204
Varsomers267607204
Maprs267607204
PheGenIrs267607204
hapmaprs267607204
1000 genomesrs267607204
hgdprs267607204
ensemblrs267607204
gopubmedrs267607204
geneviewrs267607204
scholarrs267607204
googlers267607204
pharmgkbrs267607204
gwascentralrs267607204
openSNPrs267607204
23andMers267607204
23andMe allrs267607204
SNP Nexus

SNPshotrs267607204
SNPdbers267607204
MSV3drs267607204
GWAS Ctlgrs267607204
Max Magnitude0
ClinVar
Risk rs267607204(A;A)
Alt rs267607204(A;A)
Reference rs267607204(C;C)
Significance Pathogenic
Disease Cerebral cavernous malformations 1 Cerebral cavernous malformation
Variation info
Gene KRIT1
CLNDBN Cerebral cavernous malformations 1 Cerebral cavernous malformation
Reversed 1
HGVS NC_000007.13:g.91863765G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006082.2, RCV000239438.1,