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rs876660642

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660642(-;-)
Make rs876660642(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17022660
GeneSDHB
is asnp
is mentioned by
dbSNPrs876660642
ebirs876660642
HLIrs876660642
Exacrs876660642
Varsomers876660642
Maprs876660642
PheGenIrs876660642
hapmaprs876660642
1000 genomesrs876660642
hgdprs876660642
ensemblrs876660642
gopubmedrs876660642
geneviewrs876660642
scholarrs876660642
googlers876660642
pharmgkbrs876660642
gwascentralrs876660642
openSNPrs876660642
23andMers876660642
23andMe allrs876660642
SNP Nexus

SNPshotrs876660642
SNPdbers876660642
MSV3drs876660642
GWAS Ctlgrs876660642
Max Magnitude0
ClinVar
Risk rs876660642(;)
Alt rs876660642(;)
Reference rs876660642(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHB
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.17349155delA
CLNSRC
CLNACC RCV000221959.1,