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rs1057518170

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs1057518170(-;-)
Make rs1057518170(-;AT)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position151424959
GenePOGZ
is asnp
is mentioned by
dbSNPrs1057518170
dbSNP (old)rs1057518170
ClinGenrs1057518170
ebirs1057518170
HLIrs1057518170
Exacrs1057518170
Gnomadrs1057518170
Varsomers1057518170
Maprs1057518170
PheGenIrs1057518170
Biobankrs1057518170
1000 genomesrs1057518170
hgdprs1057518170
ensemblrs1057518170
gopubmedrs1057518170
geneviewrs1057518170
scholarrs1057518170
googlers1057518170
pharmgkbrs1057518170
gwascentralrs1057518170
openSNPrs1057518170
23andMers1057518170
23andMe allrs1057518170
SNPshotrs1057518170
SNPdbers1057518170
MSV3drs1057518170
GWAS Ctlgrs1057518170
Max Magnitude0
ClinVar
Risk rs1057518170(-;-)
Alt rs1057518170(-;-)
Reference Rs1057518170(AT;AT)
Significance Pathogenic
Disease not provided dysmorphy intellectual deficiency
Variation info
Gene POGZ
CLNDBN not provided dysmorphy intellectual deficiency
Reversed 1
HGVS NC_000001.10:g.151397435_151397436delAT
CLNSRC
CLNACC RCV000414359.1, RCV000415179.1,