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rs1057517819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517819(C;C)
Make rs1057517819(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position25812764
GeneSELENON
is asnp
is mentioned by
dbSNPrs1057517819
dbSNP (old)rs1057517819
ClinGenrs1057517819
ebirs1057517819
HLIrs1057517819
Exacrs1057517819
Gnomadrs1057517819
Varsomers1057517819
LitVarrs1057517819
Maprs1057517819
PheGenIrs1057517819
Biobankrs1057517819
1000 genomesrs1057517819
hgdprs1057517819
ensemblrs1057517819
gopubmedrs1057517819
geneviewrs1057517819
scholarrs1057517819
googlers1057517819
pharmgkbrs1057517819
gwascentralrs1057517819
openSNPrs1057517819
23andMers1057517819
23andMe allrs1057517819
SNPshotrs1057517819
SNPdbers1057517819
MSV3drs1057517819
GWAS Ctlgrs1057517819
Max Magnitude0
ClinVar
Risk rs1057517819(C;C)
Alt rs1057517819(C;C)
Reference Rs1057517819(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SELENON
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.26139255G>C
CLNSRC
CLNACC RCV000413433.1,