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rs1057517804

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517804(-;G)
Make rs1057517804(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position120816542
GenePRDM5
is asnp
is mentioned by
dbSNPrs1057517804
dbSNP (old)rs1057517804
ClinGenrs1057517804
ebirs1057517804
HLIrs1057517804
Exacrs1057517804
Gnomadrs1057517804
Varsomers1057517804
LitVarrs1057517804
Maprs1057517804
PheGenIrs1057517804
Biobankrs1057517804
1000 genomesrs1057517804
hgdprs1057517804
ensemblrs1057517804
gopubmedrs1057517804
geneviewrs1057517804
scholarrs1057517804
googlers1057517804
pharmgkbrs1057517804
gwascentralrs1057517804
openSNPrs1057517804
23andMers1057517804
23andMe allrs1057517804
SNPshotrs1057517804
SNPdbers1057517804
MSV3drs1057517804
GWAS Ctlgrs1057517804
Max Magnitude0
ClinVar
Risk rs1057517804(G;G)
Alt rs1057517804(G;G)
Reference Rs1057517804(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRDM5
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.121737698dupC
CLNSRC
CLNACC RCV000413935.1,