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

rs730881037

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881037(A;C)
Make rs730881037(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39056703
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881037
ebirs730881037
HLIrs730881037
Exacrs730881037
Varsomers730881037
Maprs730881037
PheGenIrs730881037
hapmaprs730881037
1000 genomesrs730881037
hgdprs730881037
ensemblrs730881037
gopubmedrs730881037
geneviewrs730881037
scholarrs730881037
googlers730881037
pharmgkbrs730881037
gwascentralrs730881037
openSNPrs730881037
23andMers730881037
23andMe allrs730881037
SNP Nexus

SNPshotrs730881037
SNPdbers730881037
MSV3drs730881037
GWAS Ctlgrs730881037
Max Magnitude0
ClinVar
Risk rs730881037(C;C)
Alt rs730881037(C;C)
Reference rs730881037(A;A)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene SOS1
CLNDBN Rasopathy
Reversed 1
HGVS NC_000002.11:g.39283844T>G
CLNSRC
CLNACC RCV000159151.1,