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rs869312687

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312687(A;C)
Make rs869312687(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position155910695
GeneRIT1
is asnp
is mentioned by
dbSNPrs869312687
ebirs869312687
HLIrs869312687
Exacrs869312687
Varsomers869312687
Maprs869312687
PheGenIrs869312687
hapmaprs869312687
1000 genomesrs869312687
hgdprs869312687
ensemblrs869312687
gopubmedrs869312687
geneviewrs869312687
scholarrs869312687
googlers869312687
pharmgkbrs869312687
gwascentralrs869312687
openSNPrs869312687
23andMers869312687
23andMe allrs869312687
SNP Nexus

SNPshotrs869312687
SNPdbers869312687
MSV3drs869312687
GWAS Ctlgrs869312687
Max Magnitude0
ClinVar
Risk rs869312687(C;C)
Alt rs869312687(C;C)
Reference rs869312687(A;A)
Significance Pathogenic
Disease Noonan syndrome 8
Variation info
Gene RIT1
CLNDBN Noonan syndrome 8
Reversed 1
HGVS NC_000001.10:g.155880486T>G
CLNSRC
CLNACC RCV000209835.2,