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rs730881045

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881045(A;A)
Make rs730881045(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39022784
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881045
ebirs730881045
HLIrs730881045
Exacrs730881045
Varsomers730881045
Maprs730881045
PheGenIrs730881045
hapmaprs730881045
1000 genomesrs730881045
hgdprs730881045
ensemblrs730881045
gopubmedrs730881045
geneviewrs730881045
scholarrs730881045
googlers730881045
pharmgkbrs730881045
gwascentralrs730881045
openSNPrs730881045
23andMers730881045
23andMe allrs730881045
SNP Nexus

SNPshotrs730881045
SNPdbers730881045
MSV3drs730881045
GWAS Ctlgrs730881045
Max Magnitude0
ClinVar
Risk rs730881045(A;A)
Alt rs730881045(A;A)
Reference rs730881045(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39249925A>T
CLNSRC
CLNACC RCV000159171.1,