Have questions? Visit https://www.reddit.com/r/SNPedia

rs11551664

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11551664(C;T)
Make rs11551664(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1390985
GeneNDUFS7
is asnp
is mentioned by
dbSNPrs11551664
ebirs11551664
HLIrs11551664
Exacrs11551664
Varsomers11551664
Maprs11551664
PheGenIrs11551664
hapmaprs11551664
1000 genomesrs11551664
hgdprs11551664
ensemblrs11551664
gopubmedrs11551664
geneviewrs11551664
scholarrs11551664
googlers11551664
pharmgkbrs11551664
gwascentralrs11551664
openSNPrs11551664
23andMers11551664
23andMe allrs11551664
SNP Nexus

SNPshotrs11551664
SNPdbers11551664
MSV3drs11551664
GWAS Ctlgrs11551664
Max Magnitude0
ClinVar
Risk rs11551664(T;T)
Alt rs11551664(T;T)
Reference rs11551664(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS7
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1390984C>T
CLNSRC
CLNACC RCV000195624.2,