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rs730881054

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881054(A;A)
Make rs730881054(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39058765
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881054
ebirs730881054
HLIrs730881054
Exacrs730881054
Varsomers730881054
Maprs730881054
PheGenIrs730881054
hapmaprs730881054
1000 genomesrs730881054
hgdprs730881054
ensemblrs730881054
gopubmedrs730881054
geneviewrs730881054
scholarrs730881054
googlers730881054
pharmgkbrs730881054
gwascentralrs730881054
openSNPrs730881054
23andMers730881054
23andMe allrs730881054
SNP Nexus

SNPshotrs730881054
SNPdbers730881054
MSV3drs730881054
GWAS Ctlgrs730881054
Max Magnitude0
ClinVar
Risk rs730881054(A;A)
Alt rs730881054(A;A)
Reference rs730881054(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39285906A>T
CLNSRC
CLNACC RCV000159187.2,