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rs869025196

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025196(C;T)
Make rs869025196(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position155904489
GeneRIT1
is asnp
is mentioned by
dbSNPrs869025196
ebirs869025196
HLIrs869025196
Exacrs869025196
Varsomers869025196
Maprs869025196
PheGenIrs869025196
hapmaprs869025196
1000 genomesrs869025196
hgdprs869025196
ensemblrs869025196
gopubmedrs869025196
geneviewrs869025196
scholarrs869025196
googlers869025196
pharmgkbrs869025196
gwascentralrs869025196
openSNPrs869025196
23andMers869025196
23andMe allrs869025196
SNP Nexus

SNPshotrs869025196
SNPdbers869025196
MSV3drs869025196
GWAS Ctlgrs869025196
Max Magnitude0
ClinVar
Risk rs869025196(T;T)
Alt rs869025196(T;T)
Reference rs869025196(C;C)
Significance Probable-Pathogenic
Disease Noonan syndrome
Variation info
Gene RIT1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000001.10:g.155874280G>A
CLNSRC
CLNACC RCV000207351.1,