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rs35082957

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35082957(A;A)
Make rs35082957(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position2406553
GenePEX10
is asnp
is mentioned by
dbSNPrs35082957
ebirs35082957
HLIrs35082957
Exacrs35082957
Varsomers35082957
Maprs35082957
PheGenIrs35082957
hapmaprs35082957
1000 genomesrs35082957
hgdprs35082957
ensemblrs35082957
gopubmedrs35082957
geneviewrs35082957
scholarrs35082957
googlers35082957
pharmgkbrs35082957
gwascentralrs35082957
openSNPrs35082957
23andMers35082957
23andMe allrs35082957
SNP Nexus

SNPshotrs35082957
SNPdbers35082957
MSV3drs35082957
GWAS Ctlgrs35082957
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs35082957(A;A)
Alt rs35082957(A;A)
Reference rs35082957(G;G)
Significance Untested
Disease
Variation info
Gene PEX10
CLNDBN
Reversed 1
HGVS NC_000001.10:g.2337992C>T
CLNSRC
CLNACC