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rs200245469

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200245469(A;A)
Make rs200245469(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17022724
GeneSDHB
is asnp
is mentioned by
dbSNPrs200245469
ebirs200245469
HLIrs200245469
Exacrs200245469
Varsomers200245469
Maprs200245469
PheGenIrs200245469
hapmaprs200245469
1000 genomesrs200245469
hgdprs200245469
ensemblrs200245469
gopubmedrs200245469
geneviewrs200245469
scholarrs200245469
googlers200245469
pharmgkbrs200245469
gwascentralrs200245469
openSNPrs200245469
23andMers200245469
23andMe allrs200245469
SNP Nexus

SNPshotrs200245469
SNPdbers200245469
MSV3drs200245469
GWAS Ctlgrs200245469
Max Magnitude0
ClinVar
Risk rs200245469(A,C;A,C)
Alt rs200245469(A,C;A,C)
Reference rs200245469(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.17349219G>A
CLNSRC
CLNACC RCV000162444.1,