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rs869025197

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025197(C;C)
Make rs869025197(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position155904475
GeneRIT1
is asnp
is mentioned by
dbSNPrs869025197
ebirs869025197
HLIrs869025197
Exacrs869025197
Varsomers869025197
Maprs869025197
PheGenIrs869025197
hapmaprs869025197
1000 genomesrs869025197
hgdprs869025197
ensemblrs869025197
gopubmedrs869025197
geneviewrs869025197
scholarrs869025197
googlers869025197
pharmgkbrs869025197
gwascentralrs869025197
openSNPrs869025197
23andMers869025197
23andMe allrs869025197
SNP Nexus

SNPshotrs869025197
SNPdbers869025197
MSV3drs869025197
GWAS Ctlgrs869025197
Max Magnitude0
ClinVar
Risk rs869025197(C;C)
Alt rs869025197(C;C)
Reference rs869025197(T;T)
Significance Pathogenic
Disease Noonan syndrome
Variation info
Gene RIT1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000001.10:g.155874266A>G
CLNSRC
CLNACC RCV000207342.1,