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rs1057518113

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518113(A;A)
Make rs1057518113(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position151427984
GenePOGZ
is asnp
is mentioned by
dbSNPrs1057518113
dbSNP (old)rs1057518113
ClinGenrs1057518113
ebirs1057518113
HLIrs1057518113
Exacrs1057518113
Gnomadrs1057518113
Varsomers1057518113
Maprs1057518113
PheGenIrs1057518113
Biobankrs1057518113
1000 genomesrs1057518113
hgdprs1057518113
ensemblrs1057518113
gopubmedrs1057518113
geneviewrs1057518113
scholarrs1057518113
googlers1057518113
pharmgkbrs1057518113
gwascentralrs1057518113
openSNPrs1057518113
23andMers1057518113
23andMe allrs1057518113
SNPshotrs1057518113
SNPdbers1057518113
MSV3drs1057518113
GWAS Ctlgrs1057518113
Max Magnitude0
ClinVar
Risk rs1057518113(A;A)
Alt rs1057518113(A;A)
Reference Rs1057518113(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POGZ
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.151400460C>T
CLNSRC
CLNACC RCV000413150.1,