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rs387906358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs387906358(-;-)
Make rs387906358(-;TC)
ReferenceGRCh38 38.1/141
Chromosome11
Position112088888
GeneSDHD
is asnp
is mentioned by
dbSNPrs387906358
ebirs387906358
HLIrs387906358
Exacrs387906358
Varsomers387906358
Maprs387906358
PheGenIrs387906358
hapmaprs387906358
1000 genomesrs387906358
hgdprs387906358
ensemblrs387906358
gopubmedrs387906358
geneviewrs387906358
scholarrs387906358
googlers387906358
pharmgkbrs387906358
gwascentralrs387906358
openSNPrs387906358
23andMers387906358
23andMe allrs387906358
SNP Nexus

SNPshotrs387906358
SNPdbers387906358
MSV3drs387906358
GWAS Ctlgrs387906358
Max Magnitude0
ClinVar
Risk rs387906358(;)
Alt rs387906358(;)
Reference rs387906358(TC;TC)
Significance Pathogenic
Disease Paragangliomas 1 with sensorineural hearing loss
Variation info
Gene SDHD
CLNDBN Paragangliomas 1 with sensorineural hearing loss
Reversed 0
HGVS NC_000011.9:g.111959612_111959613delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007313.2,