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rs730881042

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881042(A;G)
Make rs730881042(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39023157
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881042
ebirs730881042
HLIrs730881042
Exacrs730881042
Varsomers730881042
Maprs730881042
PheGenIrs730881042
hapmaprs730881042
1000 genomesrs730881042
hgdprs730881042
ensemblrs730881042
gopubmedrs730881042
geneviewrs730881042
scholarrs730881042
googlers730881042
pharmgkbrs730881042
gwascentralrs730881042
openSNPrs730881042
23andMers730881042
23andMe allrs730881042
SNP Nexus

SNPshotrs730881042
SNPdbers730881042
MSV3drs730881042
GWAS Ctlgrs730881042
Max Magnitude0
ClinVar
Risk rs730881042(G;G)
Alt rs730881042(G;G)
Reference rs730881042(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39250298T>C
CLNSRC
CLNACC RCV000159160.2,