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rs727503904

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503904(A;A)
Make rs727503904(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position128945857
GeneDOLK, NUP188
is asnp
is mentioned by
dbSNPrs727503904
ebirs727503904
HLIrs727503904
Exacrs727503904
Varsomers727503904
Maprs727503904
PheGenIrs727503904
hapmaprs727503904
1000 genomesrs727503904
hgdprs727503904
ensemblrs727503904
gopubmedrs727503904
geneviewrs727503904
scholarrs727503904
googlers727503904
pharmgkbrs727503904
gwascentralrs727503904
openSNPrs727503904
23andMers727503904
23andMe allrs727503904
SNP Nexus

SNPshotrs727503904
SNPdbers727503904
MSV3drs727503904
GWAS Ctlgrs727503904
Max Magnitude0
ClinVar
Risk rs727503904(A;A)
Alt rs727503904(A;A)
Reference rs727503904(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DOLK NUP188
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.131708136G>T
CLNSRC
CLNACC RCV000153162.3,