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rs730881046

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881046(A;A)
Make rs730881046(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39022782
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881046
ebirs730881046
HLIrs730881046
Exacrs730881046
Varsomers730881046
Maprs730881046
PheGenIrs730881046
hapmaprs730881046
1000 genomesrs730881046
hgdprs730881046
ensemblrs730881046
gopubmedrs730881046
geneviewrs730881046
scholarrs730881046
googlers730881046
pharmgkbrs730881046
gwascentralrs730881046
openSNPrs730881046
23andMers730881046
23andMe allrs730881046
SNP Nexus

SNPshotrs730881046
SNPdbers730881046
MSV3drs730881046
GWAS Ctlgrs730881046
Max Magnitude0
ClinVar
Risk rs730881046(A;A)
Alt rs730881046(A;A)
Reference rs730881046(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39249923G>T
CLNSRC
CLNACC RCV000159173.1,