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rs746993242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs746993242(G;G)
Make rs746993242(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position4901077
GeneCHRNE, C17orf107
is asnp
is mentioned by
dbSNPrs746993242
dbSNP (classic)rs746993242
ClinGenrs746993242
ebirs746993242
HLIrs746993242
Exacrs746993242
Gnomadrs746993242
Varsomers746993242
LitVarrs746993242
Maprs746993242
PheGenIrs746993242
Biobankrs746993242
1000 genomesrs746993242
hgdprs746993242
ensemblrs746993242
geneviewrs746993242
scholarrs746993242
googlers746993242
pharmgkbrs746993242
gwascentralrs746993242
openSNPrs746993242
23andMers746993242
SNPshotrs746993242
SNPdbers746993242
MSV3drs746993242
GWAS Ctlgrs746993242
Max Magnitude0
ClinVar
Risk rs746993242(G;G)
Alt rs746993242(G;G)
Reference Rs746993242(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C17orf107 CHRNE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.4804372T>G
CLNSRC
CLNACC RCV000489085.1,