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rs104894702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894702(A;A)
Make rs104894702(A;T)
ReferenceGRCh37 37.1/132
Chromosome19
Position920746
GeneKISS1R
is asnp
is mentioned by
dbSNPrs104894702
ebirs104894702
HLIrs104894702
Exacrs104894702
Varsomers104894702
Maprs104894702
PheGenIrs104894702
hapmaprs104894702
1000 genomesrs104894702
hgdprs104894702
ensemblrs104894702
gopubmedrs104894702
geneviewrs104894702
scholarrs104894702
googlers104894702
pharmgkbrs104894702
gwascentralrs104894702
openSNPrs104894702
23andMers104894702
23andMe allrs104894702
SNP Nexus

SNPshotrs104894702
SNPdbers104894702
MSV3drs104894702
GWAS Ctlgrs104894702
Max Magnitude0
OMIM604161
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894702(A;A)
Alt rs104894702(A;A)
Reference rs104894702(T;T)
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.920746T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030880.5,