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rs727505093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505093(G;G)
Make rs727505093(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position39014838
GeneSOS1
is asnp
is mentioned by
dbSNPrs727505093
dbSNP (classic)rs727505093
ClinGenrs727505093
ebirs727505093
HLIrs727505093
Exacrs727505093
Gnomadrs727505093
Varsomers727505093
LitVarrs727505093
Maprs727505093
PheGenIrs727505093
Biobankrs727505093
1000 genomesrs727505093
hgdprs727505093
ensemblrs727505093
geneviewrs727505093
scholarrs727505093
googlers727505093
pharmgkbrs727505093
gwascentralrs727505093
openSNPrs727505093
23andMers727505093
SNPshotrs727505093
SNPdbers727505093
MSV3drs727505093
GWAS Ctlgrs727505093
Max Magnitude0
ClinVar
Risk rs727505093(G;G)
Alt rs727505093(G;G)
Reference Rs727505093(T;T)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene SOS1
CLNDBN not specified not provided
Reversed 1
HGVS NC_000002.11:g.39241979A>C
CLNSRC
CLNACC RCV000156537.1, RCV000414349.1,