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rs376142095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376142095(C;T)
Make rs376142095(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position5302452
GenePROKR2
is asnp
is mentioned by
dbSNPrs376142095
ebirs376142095
HLIrs376142095
Exacrs376142095
Varsomers376142095
Maprs376142095
PheGenIrs376142095
hapmaprs376142095
1000 genomesrs376142095
hgdprs376142095
ensemblrs376142095
gopubmedrs376142095
geneviewrs376142095
scholarrs376142095
googlers376142095
pharmgkbrs376142095
gwascentralrs376142095
openSNPrs376142095
23andMers376142095
23andMe allrs376142095
SNP Nexus

SNPshotrs376142095
SNPdbers376142095
MSV3drs376142095
GWAS Ctlgrs376142095
Max Magnitude0
ClinVar
Risk rs376142095(T;T)
Alt rs376142095(T;T)
Reference rs376142095(C;C)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 3 without anosmia
Variation info
Gene PROKR2
CLNDBN Hypogonadotropic hypogonadism 3 without anosmia
Reversed 0
HGVS NC_000020.10:g.5283098C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144715.3,