Have questions? Visit https://www.reddit.com/r/SNPedia

rs869320687

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320687(C;G)
Make rs869320687(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position50161551
GeneSOS2
is asnp
is mentioned by
dbSNPrs869320687
ebirs869320687
HLIrs869320687
Exacrs869320687
Varsomers869320687
Maprs869320687
PheGenIrs869320687
hapmaprs869320687
1000 genomesrs869320687
hgdprs869320687
ensemblrs869320687
gopubmedrs869320687
geneviewrs869320687
scholarrs869320687
googlers869320687
pharmgkbrs869320687
gwascentralrs869320687
openSNPrs869320687
23andMers869320687
23andMe allrs869320687
SNP Nexus

SNPshotrs869320687
SNPdbers869320687
MSV3drs869320687
GWAS Ctlgrs869320687
Max Magnitude0
ClinVar
Risk rs869320687(G;G)
Alt rs869320687(G;G)
Reference rs869320687(C;C)
Significance Pathogenic
Disease Noonan syndrome 9 not provided
Variation info
Gene SOS2
CLNDBN Noonan syndrome 9 not provided
Reversed 1
HGVS NC_000014.8:g.50628269G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000191030.2, RCV000224178.1,