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rs786205600

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205600(C;C)
Make rs786205600(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136497539
GeneNOTCH1
is asnp
is mentioned by
dbSNPrs786205600
ebirs786205600
HLIrs786205600
Exacrs786205600
Varsomers786205600
Maprs786205600
PheGenIrs786205600
hapmaprs786205600
1000 genomesrs786205600
hgdprs786205600
ensemblrs786205600
gopubmedrs786205600
geneviewrs786205600
scholarrs786205600
googlers786205600
pharmgkbrs786205600
gwascentralrs786205600
openSNPrs786205600
23andMers786205600
23andMe allrs786205600
SNP Nexus

SNPshotrs786205600
SNPdbers786205600
MSV3drs786205600
GWAS Ctlgrs786205600
Max Magnitude0
ClinVar
Risk rs786205600(C;C)
Alt rs786205600(C;C)
Reference rs786205600(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.139391991A>G
CLNSRC
CLNACC RCV000171429.1,