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rs1057518600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518600(-;AG)
Make rs1057518600(AG;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position196238835
GenePCYT1A
is asnp
is mentioned by
dbSNPrs1057518600
dbSNP (old)rs1057518600
ClinGenrs1057518600
ebirs1057518600
HLIrs1057518600
Exacrs1057518600
Gnomadrs1057518600
Varsomers1057518600
Maprs1057518600
PheGenIrs1057518600
Biobankrs1057518600
1000 genomesrs1057518600
hgdprs1057518600
ensemblrs1057518600
gopubmedrs1057518600
geneviewrs1057518600
scholarrs1057518600
googlers1057518600
pharmgkbrs1057518600
gwascentralrs1057518600
openSNPrs1057518600
23andMers1057518600
23andMe allrs1057518600
SNPshotrs1057518600
SNPdbers1057518600
MSV3drs1057518600
GWAS Ctlgrs1057518600
Max Magnitude0
ClinVar
Risk rs1057518600(AG;AG)
Alt rs1057518600(AG;AG)
Reference Rs1057518600(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCYT1A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.195965707_195965708dupCT
CLNSRC
CLNACC RCV000414367.1,