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rs869025192

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025192(C;C)
Make rs869025192(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position155904499
GeneRIT1
is asnp
is mentioned by
dbSNPrs869025192
ebirs869025192
HLIrs869025192
Exacrs869025192
Varsomers869025192
Maprs869025192
PheGenIrs869025192
hapmaprs869025192
1000 genomesrs869025192
hgdprs869025192
ensemblrs869025192
gopubmedrs869025192
geneviewrs869025192
scholarrs869025192
googlers869025192
pharmgkbrs869025192
gwascentralrs869025192
openSNPrs869025192
23andMers869025192
23andMe allrs869025192
SNP Nexus

SNPshotrs869025192
SNPdbers869025192
MSV3drs869025192
GWAS Ctlgrs869025192
Max Magnitude0
ClinVar
Risk rs869025192(C;C)
Alt rs869025192(C;C)
Reference rs869025192(G;G)
Significance Pathogenic
Disease Noonan syndrome
Variation info
Gene RIT1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000001.10:g.155874290C>G
CLNSRC
CLNACC RCV000207347.1,