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rs730881043

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881043(A;A)
Make rs730881043(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39023043
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881043
ebirs730881043
HLIrs730881043
Exacrs730881043
Varsomers730881043
Maprs730881043
PheGenIrs730881043
hapmaprs730881043
1000 genomesrs730881043
hgdprs730881043
ensemblrs730881043
gopubmedrs730881043
geneviewrs730881043
scholarrs730881043
googlers730881043
pharmgkbrs730881043
gwascentralrs730881043
openSNPrs730881043
23andMers730881043
23andMe allrs730881043
SNP Nexus

SNPshotrs730881043
SNPdbers730881043
MSV3drs730881043
GWAS Ctlgrs730881043
Max Magnitude0
ClinVar
Risk rs730881043(A;A)
Alt rs730881043(A;A)
Reference rs730881043(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39250184A>T
CLNSRC
CLNACC RCV000159167.1,