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rs886041572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 5.2 Cerebral cavernous angioma associated mutation; variable penetrance
Make rs886041572(T;T)
Chromosome7
Position92214655
GeneKRIT1
is asnp
is mentioned by
dbSNPrs886041572
dbSNP (classic)rs886041572
ClinGenrs886041572
ebirs886041572
HLIrs886041572
Exacrs886041572
Gnomadrs886041572
Varsomers886041572
LitVarrs886041572
Maprs886041572
PheGenIrs886041572
Biobankrs886041572
1000 genomesrs886041572
hgdprs886041572
ensemblrs886041572
geneviewrs886041572
scholarrs886041572
googlers886041572
pharmgkbrs886041572
gwascentralrs886041572
openSNPrs886041572
23andMers886041572
SNPshotrs886041572
SNPdbers886041572
MSV3drs886041572
GWAS Ctlgrs886041572
Max Magnitude5.2

aka c.1685dupT (p.Tyr563Leufs)

ClinVar
Risk rs886041572(T;T)
Alt rs886041572(T;T)
Reference Rs886041572(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KRIT1
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.91843970dupA
CLNSRC
CLNACC RCV000291180.1,