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rs775605330

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775605330(A;C)
Make rs775605330(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position61073128
GeneNDUFAF2
is asnp
is mentioned by
dbSNPrs775605330
ebirs775605330
HLIrs775605330
Exacrs775605330
Varsomers775605330
Maprs775605330
PheGenIrs775605330
hapmaprs775605330
1000 genomesrs775605330
hgdprs775605330
ensemblrs775605330
gopubmedrs775605330
geneviewrs775605330
scholarrs775605330
googlers775605330
pharmgkbrs775605330
gwascentralrs775605330
openSNPrs775605330
23andMers775605330
23andMe allrs775605330
SNP Nexus

SNPshotrs775605330
SNPdbers775605330
MSV3drs775605330
GWAS Ctlgrs775605330
Max Magnitude0
ClinVar
Risk rs775605330(C;C)
Alt rs775605330(C;C)
Reference rs775605330(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFAF2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.60368955A>C
CLNSRC
CLNACC RCV000197862.1,