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rs1064797150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position100993223
GeneC10orf2, TWNK
is asnp
is mentioned by
dbSNPrs1064797150
dbSNP (old)rs1064797150
ClinGenrs1064797150
ebirs1064797150
HLIrs1064797150
Exacrs1064797150
Gnomadrs1064797150
Varsomers1064797150
Maprs1064797150
PheGenIrs1064797150
Biobankrs1064797150
1000 genomesrs1064797150
hgdprs1064797150
ensemblrs1064797150
gopubmedrs1064797150
geneviewrs1064797150
scholarrs1064797150
googlers1064797150
pharmgkbrs1064797150
gwascentralrs1064797150
openSNPrs1064797150
23andMers1064797150
23andMe allrs1064797150
SNPshotrs1064797150
SNPdbers1064797150
MSV3drs1064797150
GWAS Ctlgrs1064797150
Max Magnitude0
ClinVar
Risk rs1064797150(T;T)
Alt rs1064797150(T;T)
Reference Rs1064797150(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TWNK C10orf2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102752980C>T
CLNSRC
CLNACC RCV000488219.1,