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rs869025195

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025195(A;C)
Make rs869025195(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position155904493
GeneRIT1
is asnp
is mentioned by
dbSNPrs869025195
ebirs869025195
HLIrs869025195
Exacrs869025195
Varsomers869025195
Maprs869025195
PheGenIrs869025195
hapmaprs869025195
1000 genomesrs869025195
hgdprs869025195
ensemblrs869025195
gopubmedrs869025195
geneviewrs869025195
scholarrs869025195
googlers869025195
pharmgkbrs869025195
gwascentralrs869025195
openSNPrs869025195
23andMers869025195
23andMe allrs869025195
SNP Nexus

SNPshotrs869025195
SNPdbers869025195
MSV3drs869025195
GWAS Ctlgrs869025195
Max Magnitude0
ClinVar
Risk rs869025195(C;C)
Alt rs869025195(C;C)
Reference rs869025195(A;A)
Significance Pathogenic
Disease Noonan syndrome
Variation info
Gene RIT1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000001.10:g.155874284T>G
CLNSRC
CLNACC RCV000207345.1,