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rs78310959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs78310959(A;G)
Make rs78310959(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position142314648
GeneSPRY4
is asnp
is mentioned by
dbSNPrs78310959
ebirs78310959
HLIrs78310959
Exacrs78310959
Varsomers78310959
Maprs78310959
PheGenIrs78310959
hapmaprs78310959
1000 genomesrs78310959
hgdprs78310959
ensemblrs78310959
gopubmedrs78310959
geneviewrs78310959
scholarrs78310959
googlers78310959
pharmgkbrs78310959
gwascentralrs78310959
openSNPrs78310959
23andMers78310959
23andMe allrs78310959
SNP Nexus

SNPshotrs78310959
SNPdbers78310959
MSV3drs78310959
GWAS Ctlgrs78310959
Max Magnitude0
ClinVar
Risk rs78310959(G;G)
Alt rs78310959(G;G)
Reference rs78310959(A;A)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 17 with or without anosmia
Variation info
Gene SPRY4
CLNDBN Hypogonadotropic hypogonadism 17 with or without anosmia
Reversed 1
HGVS NC_000005.9:g.141694213T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000043614.2,