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rs6256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs6256(A;A)
Make rs6256(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position13492506
GenePTH
is asnp
is mentioned by
dbSNPrs6256
ebirs6256
HLIrs6256
Exacrs6256
Varsomers6256
Maprs6256
PheGenIrs6256
hapmaprs6256
1000 genomesrs6256
hgdprs6256
ensemblrs6256
gopubmedrs6256
geneviewrs6256
scholarrs6256
googlers6256
pharmgkbrs6256
gwascentralrs6256
openSNPrs6256
23andMers6256
23andMe allrs6256
SNP Nexus

SNPshotrs6256
SNPdbers6256
MSV3drs6256
GWAS Ctlgrs6256
GMAF0.1272
Max Magnitude0
? (A;A) (A;C) (C;C) 28
OMIM168450
Desc
Variant0004
Relatedalso


[PMID 21637951] A common variant in the adiponectin gene and polycystic ovary syndrome risk


ClinVar
Risk rs6256(A,T;A,T)
Alt rs6256(A,T;A,T)
Reference rs6256(C;C)
Significance Pathogenic
Disease Primary hyperparathyroidism
Variation info
Gene PTH
CLNDBN Primary hyperparathyroidism
Reversed 1
HGVS NC_000011.9:g.13514053G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014767.25,



[PMID 18551993] SNP combinations in chromosome-wide genes are associated with bone mineral density in Taiwanese women.