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rs370241999

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370241999(A;A)
Make rs370241999(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1393226
GeneNDUFS7
is asnp
is mentioned by
dbSNPrs370241999
ebirs370241999
HLIrs370241999
Exacrs370241999
Varsomers370241999
Maprs370241999
PheGenIrs370241999
hapmaprs370241999
1000 genomesrs370241999
hgdprs370241999
ensemblrs370241999
gopubmedrs370241999
geneviewrs370241999
scholarrs370241999
googlers370241999
pharmgkbrs370241999
gwascentralrs370241999
openSNPrs370241999
23andMers370241999
23andMe allrs370241999
SNP Nexus

SNPshotrs370241999
SNPdbers370241999
MSV3drs370241999
GWAS Ctlgrs370241999
Max Magnitude0
ClinVar
Risk rs370241999(A;A)
Alt rs370241999(A;A)
Reference rs370241999(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene NDUFS7
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.1393225G>A
CLNSRC
CLNACC RCV000199158.2,