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rs1057518400

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518400(C;C)
Make rs1057518400(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position95476858
GenePTCH1
is asnp
is mentioned by
dbSNPrs1057518400
dbSNP (old)rs1057518400
ClinGenrs1057518400
ebirs1057518400
HLIrs1057518400
Exacrs1057518400
Gnomadrs1057518400
Varsomers1057518400
Maprs1057518400
PheGenIrs1057518400
Biobankrs1057518400
1000 genomesrs1057518400
hgdprs1057518400
ensemblrs1057518400
gopubmedrs1057518400
geneviewrs1057518400
scholarrs1057518400
googlers1057518400
pharmgkbrs1057518400
gwascentralrs1057518400
openSNPrs1057518400
23andMers1057518400
23andMe allrs1057518400
SNPshotrs1057518400
SNPdbers1057518400
MSV3drs1057518400
GWAS Ctlgrs1057518400
Max Magnitude0
ClinVar
Risk rs1057518400(C;C)
Alt rs1057518400(C;C)
Reference Rs1057518400(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCH1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.98239140C>G
CLNSRC
CLNACC RCV000412941.1,