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rs765835040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765835040(C;T)
Make rs765835040(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position44857158
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs765835040
dbSNP (classic)rs765835040
ClinGenrs765835040
ebirs765835040
HLIrs765835040
Exacrs765835040
Gnomadrs765835040
Varsomers765835040
LitVarrs765835040
Maprs765835040
PheGenIrs765835040
Biobankrs765835040
1000 genomesrs765835040
hgdprs765835040
ensemblrs765835040
geneviewrs765835040
scholarrs765835040
googlers765835040
pharmgkbrs765835040
gwascentralrs765835040
openSNPrs765835040
23andMers765835040
SNPshotrs765835040
SNPdbers765835040
MSV3drs765835040
GWAS Ctlgrs765835040
Max Magnitude0
ClinVar
Risk rs765835040(A;A) rs765835040(T;T)
Alt rs765835040(A;A) rs765835040(T;T)
Reference Rs765835040(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.42934526C>A
CLNSRC
CLNACC RCV000479806.1,