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rs755303686

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755303686(C;G)
Make rs755303686(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position4899385
GeneCHRNE, C17orf107
is asnp
is mentioned by
dbSNPrs755303686
dbSNP (classic)rs755303686
ClinGenrs755303686
ebirs755303686
HLIrs755303686
Exacrs755303686
Gnomadrs755303686
Varsomers755303686
LitVarrs755303686
Maprs755303686
PheGenIrs755303686
Biobankrs755303686
1000 genomesrs755303686
hgdprs755303686
ensemblrs755303686
geneviewrs755303686
scholarrs755303686
googlers755303686
pharmgkbrs755303686
gwascentralrs755303686
openSNPrs755303686
23andMers755303686
SNPshotrs755303686
SNPdbers755303686
MSV3drs755303686
GWAS Ctlgrs755303686
Max Magnitude0
ClinVar
Risk rs755303686(G;G)
Alt rs755303686(G;G)
Reference Rs755303686(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene C17orf107 CHRNE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.4802680C>G
CLNSRC
CLNACC RCV000483785.1,