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

rs797045167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045167(A;A)
Make rs797045167(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position50182521
GeneSOS2
is asnp
is mentioned by
dbSNPrs797045167
dbSNP (old)rs797045167
ClinGenrs797045167
ebirs797045167
HLIrs797045167
Exacrs797045167
Gnomadrs797045167
Varsomers797045167
Maprs797045167
PheGenIrs797045167
Biobankrs797045167
1000 genomesrs797045167
hgdprs797045167
ensemblrs797045167
gopubmedrs797045167
geneviewrs797045167
scholarrs797045167
googlers797045167
pharmgkbrs797045167
gwascentralrs797045167
openSNPrs797045167
23andMers797045167
23andMe allrs797045167
SNP Nexus

SNPshotrs797045167
SNPdbers797045167
MSV3drs797045167
GWAS Ctlgrs797045167
Max Magnitude0
ClinVar
Risk rs797045167(A;A) rs797045167(C;C)
Alt rs797045167(A;A) rs797045167(C;C)
Reference Rs797045167(T;T)
Significance Pathogenic
Disease not provided Noonan syndrome 9
Variation info
Gene SOS2
CLNDBN not provided Noonan syndrome 9
Reversed 1
HGVS NC_000014.8:g.50649239A>G; NC_000014.8:g.50649239A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000414175.1, RCV000191031.2,