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rs1057517861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517861(A;C)
Make rs1057517861(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position39023112
GeneSOS1
is asnp
is mentioned by
dbSNPrs1057517861
dbSNP (old)rs1057517861
ClinGenrs1057517861
ebirs1057517861
HLIrs1057517861
Exacrs1057517861
Gnomadrs1057517861
Varsomers1057517861
Maprs1057517861
PheGenIrs1057517861
Biobankrs1057517861
1000 genomesrs1057517861
hgdprs1057517861
ensemblrs1057517861
gopubmedrs1057517861
geneviewrs1057517861
scholarrs1057517861
googlers1057517861
pharmgkbrs1057517861
gwascentralrs1057517861
openSNPrs1057517861
23andMers1057517861
23andMe allrs1057517861
SNPshotrs1057517861
SNPdbers1057517861
MSV3drs1057517861
GWAS Ctlgrs1057517861
Max Magnitude0
ClinVar
Risk rs1057517861(C;C)
Alt rs1057517861(C;C)
Reference Rs1057517861(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39250253T>G
CLNSRC
CLNACC RCV000414005.1,