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rs1057523165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523165(A;A)
Make rs1057523165(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position223569
GeneSDHA
is asnp
is mentioned by
dbSNPrs1057523165
dbSNP (old)rs1057523165
ClinGenrs1057523165
ebirs1057523165
HLIrs1057523165
Exacrs1057523165
Gnomadrs1057523165
Varsomers1057523165
Maprs1057523165
PheGenIrs1057523165
Biobankrs1057523165
1000 genomesrs1057523165
hgdprs1057523165
ensemblrs1057523165
gopubmedrs1057523165
geneviewrs1057523165
scholarrs1057523165
googlers1057523165
pharmgkbrs1057523165
gwascentralrs1057523165
openSNPrs1057523165
23andMers1057523165
23andMe allrs1057523165
SNPshotrs1057523165
SNPdbers1057523165
MSV3drs1057523165
GWAS Ctlgrs1057523165
Max Magnitude0
ClinVar
Risk rs1057523165(A;A)
Alt rs1057523165(A;A)
Reference Rs1057523165(G;G)
Significance Probable-Pathogenic
Disease not specified Mitochondrial complex II deficiency Paragangliomas 5
Variation info
Gene SDHA
CLNDBN not specified Mitochondrial complex II deficiency Paragangliomas 5
Reversed 0
HGVS NC_000005.9:g.223684G>A
CLNSRC
CLNACC RCV000438780.1, RCV000471142.1,