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rs104894701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894701(C;T)
Make rs104894701(T;T)
ReferenceGRCh37 37.1/132
Chromosome19
Position920542
GeneKISS1R
is asnp
is mentioned by
dbSNPrs104894701
ebirs104894701
HLIrs104894701
Exacrs104894701
Varsomers104894701
Maprs104894701
PheGenIrs104894701
hapmaprs104894701
1000 genomesrs104894701
hgdprs104894701
ensemblrs104894701
gopubmedrs104894701
geneviewrs104894701
scholarrs104894701
googlers104894701
pharmgkbrs104894701
gwascentralrs104894701
openSNPrs104894701
23andMers104894701
23andMe allrs104894701
SNP Nexus

SNPshotrs104894701
SNPdbers104894701
MSV3drs104894701
GWAS Ctlgrs104894701
Max Magnitude0
OMIM604161
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894701(T;T)
Alt rs104894701(T;T)
Reference rs104894701(C;C)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 8 without anosmia
Variation info
Gene KISS1R
CLNDBN Hypogonadotropic hypogonadism 8 without anosmia
Reversed 0
HGVS NC_000019.9:g.920542C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030879.3,