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rs1064797351

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position14759902
GeneFREM1
is asnp
is mentioned by
dbSNPrs1064797351
dbSNP (old)rs1064797351
ClinGenrs1064797351
ebirs1064797351
HLIrs1064797351
Exacrs1064797351
Gnomadrs1064797351
Varsomers1064797351
Maprs1064797351
PheGenIrs1064797351
Biobankrs1064797351
1000 genomesrs1064797351
hgdprs1064797351
ensemblrs1064797351
gopubmedrs1064797351
geneviewrs1064797351
scholarrs1064797351
googlers1064797351
pharmgkbrs1064797351
gwascentralrs1064797351
openSNPrs1064797351
23andMers1064797351
23andMe allrs1064797351
SNPshotrs1064797351
SNPdbers1064797351
MSV3drs1064797351
GWAS Ctlgrs1064797351
Max Magnitude0
ClinVar
Risk rs1064797351(T;T)
Alt rs1064797351(T;T)
Reference Rs1064797351(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FREM1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.14759900C>A
CLNSRC
CLNACC RCV000488096.1,