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rs1057522004

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522004(A;G)
Make rs1057522004(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position20349047
GeneUMOD
is asnp
is mentioned by
dbSNPrs1057522004
dbSNP (old)rs1057522004
ClinGenrs1057522004
ebirs1057522004
HLIrs1057522004
Exacrs1057522004
Gnomadrs1057522004
Varsomers1057522004
Maprs1057522004
PheGenIrs1057522004
Biobankrs1057522004
1000 genomesrs1057522004
hgdprs1057522004
ensemblrs1057522004
gopubmedrs1057522004
geneviewrs1057522004
scholarrs1057522004
googlers1057522004
pharmgkbrs1057522004
gwascentralrs1057522004
openSNPrs1057522004
23andMers1057522004
23andMe allrs1057522004
SNPshotrs1057522004
SNPdbers1057522004
MSV3drs1057522004
GWAS Ctlgrs1057522004
Max Magnitude0
ClinVar
Risk rs1057522004(G;G)
Alt rs1057522004(G;G)
Reference Rs1057522004(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UMOD
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.20360369T>C
CLNSRC
CLNACC RCV000431019.1,