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rs1057517681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517681(C;T)
Make rs1057517681(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17394041
GenePADI6
is asnp
is mentioned by
dbSNPrs1057517681
dbSNP (old)rs1057517681
ClinGenrs1057517681
ebirs1057517681
HLIrs1057517681
Exacrs1057517681
Gnomadrs1057517681
Varsomers1057517681
Maprs1057517681
PheGenIrs1057517681
Biobankrs1057517681
1000 genomesrs1057517681
hgdprs1057517681
ensemblrs1057517681
gopubmedrs1057517681
geneviewrs1057517681
scholarrs1057517681
googlers1057517681
pharmgkbrs1057517681
gwascentralrs1057517681
openSNPrs1057517681
23andMers1057517681
23andMe allrs1057517681
SNPshotrs1057517681
SNPdbers1057517681
MSV3drs1057517681
GWAS Ctlgrs1057517681
Max Magnitude0
ClinVar
Risk rs1057517681(T;T)
Alt rs1057517681(T;T)
Reference Rs1057517681(C;C)
Significance Pathogenic
Disease Preimplantation embryonic lethality 2
Variation info
Gene PADI6
CLNDBN Preimplantation embryonic lethality 2
Reversed 0
HGVS NC_000001.10:g.17720537C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000412544.1,