Rs11203289

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Orientationminus
is asnp
is mentioned by
dbSNPrs11203289
PheGenIrs11203289
nextbiors11203289
hapmaprs11203289
1000 genomesrs11203289
hgdprs11203289
ensemblrs11203289
gopubmedrs11203289
geneviewrs11203289
scholarrs11203289
googlers11203289
pharmgkbrs11203289
gwascentralrs11203289
openSNPrs11203289
23andMers11203289
23andMe allrs11203289
SNP Nexus

SNPshotrs11203289
SNPdbers11203289
MSV3drs11203289
GeneSDHB
Chromosome1
Orientationminus
GMAF0.008724
Position17054012
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs11203289(C;G)
OMIM185470
Desc
Variant0014
Relatedalso


ClinVar
Risk rs11203289(G;G)
Alt rs11203289(G;G)
Reference rs11203289(C;C)
Significance 5
Disease Cowden-like syndrome, not provided, AllHighlyPenetrant
ClinVar info
Gene SDHB
CLNDBN Cowden-like syndrome, not provided, AllHighlyPenetrant
Reversed 1
CLNHGVS NC_000001.11:g.17054012G>C
CLNSRC ClinVar, OMIM Allelic Variant
CLNACC RCV000013632.16, RCV000034690.1, RCV000121999.1