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rs1057517682

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057517682(-;-)
Make rs1057517682(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17401362
GenePADI6
is asnp
is mentioned by
dbSNPrs1057517682
dbSNP (old)rs1057517682
ClinGenrs1057517682
ebirs1057517682
HLIrs1057517682
Exacrs1057517682
Gnomadrs1057517682
Varsomers1057517682
Maprs1057517682
PheGenIrs1057517682
Biobankrs1057517682
1000 genomesrs1057517682
hgdprs1057517682
ensemblrs1057517682
gopubmedrs1057517682
geneviewrs1057517682
scholarrs1057517682
googlers1057517682
pharmgkbrs1057517682
gwascentralrs1057517682
openSNPrs1057517682
23andMers1057517682
23andMe allrs1057517682
SNPshotrs1057517682
SNPdbers1057517682
MSV3drs1057517682
GWAS Ctlgrs1057517682
Max Magnitude0
ClinVar
Risk rs1057517682(-;-)
Alt rs1057517682(-;-)
Reference Rs1057517682(AG;AG)
Significance Pathogenic
Disease Preimplantation embryonic lethality 2
Variation info
Gene PADI6
CLNDBN Preimplantation embryonic lethality 2
Reversed 0
HGVS NC_000001.10:g.17727858_17727859delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000412605.1,