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rs137853192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853192(C;C)
Make rs137853192(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35995443
GeneSDHAF1
is asnp
is mentioned by
dbSNPrs137853192
ebirs137853192
HLIrs137853192
Exacrs137853192
Varsomers137853192
Maprs137853192
PheGenIrs137853192
hapmaprs137853192
1000 genomesrs137853192
hgdprs137853192
ensemblrs137853192
gopubmedrs137853192
geneviewrs137853192
scholarrs137853192
googlers137853192
pharmgkbrs137853192
gwascentralrs137853192
openSNPrs137853192
23andMers137853192
23andMe allrs137853192
SNP Nexus

SNPshotrs137853192
SNPdbers137853192
MSV3drs137853192
GWAS Ctlgrs137853192
Max Magnitude0
OMIM612848
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853192(C;C)
Alt rs137853192(C;C)
Reference rs137853192(G;G)
Significance Pathogenic
Disease Mitochondrial complex II deficiency
Variation info
Gene SDHAF1
CLNDBN Mitochondrial complex II deficiency
Reversed 0
HGVS NC_000019.9:g.36486345G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000457.2,