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rs1060503751

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1060503751(-;-)
Make rs1060503751(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17028691
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503751
dbSNP (old)rs1060503751
ClinGenrs1060503751
ebirs1060503751
HLIrs1060503751
Exacrs1060503751
Gnomadrs1060503751
Varsomers1060503751
Maprs1060503751
PheGenIrs1060503751
Biobankrs1060503751
1000 genomesrs1060503751
hgdprs1060503751
ensemblrs1060503751
gopubmedrs1060503751
geneviewrs1060503751
scholarrs1060503751
googlers1060503751
pharmgkbrs1060503751
gwascentralrs1060503751
openSNPrs1060503751
23andMers1060503751
23andMe allrs1060503751
SNPshotrs1060503751
SNPdbers1060503751
MSV3drs1060503751
GWAS Ctlgrs1060503751
Max Magnitude0
ClinVar
Risk rs1060503751(-;-)
Alt rs1060503751(-;-)
Reference Rs1060503751(CT;CT)
Significance Pathogenic
Disease Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17355186_17355187delAG
CLNSRC
CLNACC RCV000477482.1,