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rs1057517684

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517684(A;A)
Make rs1057517684(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17395663
GenePADI6
is asnp
is mentioned by
dbSNPrs1057517684
dbSNP (old)rs1057517684
ClinGenrs1057517684
ebirs1057517684
HLIrs1057517684
Exacrs1057517684
Gnomadrs1057517684
Varsomers1057517684
Maprs1057517684
PheGenIrs1057517684
Biobankrs1057517684
1000 genomesrs1057517684
hgdprs1057517684
ensemblrs1057517684
gopubmedrs1057517684
geneviewrs1057517684
scholarrs1057517684
googlers1057517684
pharmgkbrs1057517684
gwascentralrs1057517684
openSNPrs1057517684
23andMers1057517684
23andMe allrs1057517684
SNPshotrs1057517684
SNPdbers1057517684
MSV3drs1057517684
GWAS Ctlgrs1057517684
Max Magnitude0
ClinVar
Risk rs1057517684(A;A)
Alt rs1057517684(A;A)
Reference Rs1057517684(G;G)
Significance Pathogenic
Disease Preimplantation embryonic lethality 2
Variation info
Gene PADI6
CLNDBN Preimplantation embryonic lethality 2
Reversed 0
HGVS NC_000001.10:g.17722159G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412606.1,