Have questions? Visit https://www.reddit.com/r/SNPedia

rs775156958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs775156958(A;A)
Make rs775156958(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17382046
GenePADI6
is asnp
is mentioned by
dbSNPrs775156958
dbSNP (classic)rs775156958
ClinGenrs775156958
ebirs775156958
HLIrs775156958
Exacrs775156958
Gnomadrs775156958
Varsomers775156958
LitVarrs775156958
Maprs775156958
PheGenIrs775156958
Biobankrs775156958
1000 genomesrs775156958
hgdprs775156958
ensemblrs775156958
geneviewrs775156958
scholarrs775156958
googlers775156958
pharmgkbrs775156958
gwascentralrs775156958
openSNPrs775156958
23andMers775156958
SNPshotrs775156958
SNPdbers775156958
MSV3drs775156958
GWAS Ctlgrs775156958
Max Magnitude0
ClinVar
Risk rs775156958(A;A)
Alt rs775156958(A;A)
Reference Rs775156958(T;T)
Significance Pathogenic
Disease Preimplantation embryonic lethality 2
Variation info
Gene PADI6
CLNDBN Preimplantation embryonic lethality 2
Reversed 0
HGVS NC_000001.10:g.17708541T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412664.1,