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rs2075230

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2075230(C;C)
Make rs2075230(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position7583790
GeneLOC100996842, MPDU1
is asnp
is mentioned by
dbSNPrs2075230
dbSNP (old)rs2075230
ClinGenrs2075230
ebirs2075230
HLIrs2075230
Exacrs2075230
Gnomadrs2075230
Varsomers2075230
Maprs2075230
PheGenIrs2075230
Biobankrs2075230
1000 genomesrs2075230
hgdprs2075230
ensemblrs2075230
gopubmedrs2075230
geneviewrs2075230
scholarrs2075230
googlers2075230
pharmgkbrs2075230
gwascentralrs2075230
openSNPrs2075230
23andMers2075230
23andMe allrs2075230
SNP Nexus

SNPshotrs2075230
SNPdbers2075230
MSV3drs2075230
GWAS Ctlgrs2075230
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24049095]
Trait Hormone measurements
Title Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men.
Risk Allele G
P-val 1E-8
Odds Ratio .28 [0.18-0.38] unit decrease


ClinVar
Risk rs2075230(C;C) rs2075230(G;G)
Alt rs2075230(C;C) rs2075230(G;G)
Reference Rs2075230(T;T)
Significance Probable-non-pathogenic
Disease Congenital disorder of glycosylation
Variation info
Gene LOC100996842 MPDU1
CLNDBN Congenital disorder of glycosylation
Reversed 1
HGVS NC_000017.10:g.7487108A>G
CLNSRC
CLNACC RCV000263574.1,