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rs1057518206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518206(A;G)
Make rs1057518206(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position110964875
GeneSHOC2
is asnp
is mentioned by
dbSNPrs1057518206
dbSNP (old)rs1057518206
ClinGenrs1057518206
ebirs1057518206
HLIrs1057518206
Exacrs1057518206
Gnomadrs1057518206
Varsomers1057518206
Maprs1057518206
PheGenIrs1057518206
Biobankrs1057518206
1000 genomesrs1057518206
hgdprs1057518206
ensemblrs1057518206
gopubmedrs1057518206
geneviewrs1057518206
scholarrs1057518206
googlers1057518206
pharmgkbrs1057518206
gwascentralrs1057518206
openSNPrs1057518206
23andMers1057518206
23andMe allrs1057518206
SNPshotrs1057518206
SNPdbers1057518206
MSV3drs1057518206
GWAS Ctlgrs1057518206
Max Magnitude0
ClinVar
Risk rs1057518206(G;G)
Alt rs1057518206(G;G)
Reference Rs1057518206(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SHOC2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112724633A>G
CLNSRC
CLNACC RCV000413825.1,