Rs11203289

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Orientationminus
Make rs11203289(C;C)
Make rs11203289(C;G)
Make rs11203289(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position17054012
GeneSDHB
is asnp
is mentioned by
dbSNPrs11203289
Exacrs11203289
PheGenIrs11203289
nextbiors11203289
hapmaprs11203289
1000 genomesrs11203289
hgdprs11203289
ensemblrs11203289
gopubmedrs11203289
geneviewrs11203289
scholarrs11203289
googlers11203289
pharmgkbrs11203289
gwascentralrs11203289
openSNPrs11203289
23andMers11203289
23andMe allrs11203289
SNP Nexus

SNPshotrs11203289
SNPdbers11203289
MSV3drs11203289
GMAF0.008724
Max Magnitude
OMIM185470
Desc
Variant0014
Relatedalso


ClinVar
Risk rs11203289(G;G)
Alt rs11203289(G;G)
Reference rs11203289(C;C)
Significance Pathogenic
Disease Cowden-like syndrome not provided AllHighlyPenetrant Neoplastic Syndromes
Variation info
Gene SDHB
CLNDBN Cowden-like syndrome not provided AllHighlyPenetrant Neoplastic Syndromes, Hereditary
Reversed 1
HGVS NC_000001.11:g.17054012G>C
CLNSRC Ambry Genetics ClinVar OMIM Allelic Variant
CLNACC RCV000013632.16, RCV000034690.1, RCV000121999.1, RCV000128921.1,