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rs886043300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 5.2 Cerebral cavernous angioma associated mutation; variable penetrance
(G;G) 0 common in clinvar


Make rs886043300(A;A)
Chromosome7
Position92235417
GeneKRIT1
is asnp
is mentioned by
dbSNPrs886043300
dbSNP (classic)rs886043300
ClinGenrs886043300
ebirs886043300
HLIrs886043300
Exacrs886043300
Gnomadrs886043300
Varsomers886043300
LitVarrs886043300
Maprs886043300
PheGenIrs886043300
Biobankrs886043300
1000 genomesrs886043300
hgdprs886043300
ensemblrs886043300
geneviewrs886043300
scholarrs886043300
googlers886043300
pharmgkbrs886043300
gwascentralrs886043300
openSNPrs886043300
23andMers886043300
SNPshotrs886043300
SNPdbers886043300
MSV3drs886043300
GWAS Ctlgrs886043300
Max Magnitude5.2

aka c.715C>T (p.Gln239Ter)

ClinVar
Risk rs886043300(A;A)
Alt rs886043300(A;A)
Reference Rs886043300(G;G)
Significance Pathogenic
Disease Cerebral cavernous malformation
Variation info
Gene KRIT1
CLNDBN Cerebral cavernous malformation
Reversed 0
HGVS NC_000007.13:g.91864731G>A
CLNSRC
CLNACC RCV000392041.1,