Have questions? Visit https://www.reddit.com/r/SNPedia

rs763195944

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs763195944(-;-)
Make rs763195944(-;C)
Make rs763195944(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position23566257
GeneMKRN3
is asnp
is mentioned by
dbSNPrs763195944
ebirs763195944
HLIrs763195944
Exacrs763195944
Varsomers763195944
Maprs763195944
PheGenIrs763195944
hapmaprs763195944
1000 genomesrs763195944
hgdprs763195944
ensemblrs763195944
gopubmedrs763195944
geneviewrs763195944
scholarrs763195944
googlers763195944
pharmgkbrs763195944
gwascentralrs763195944
openSNPrs763195944
23andMers763195944
23andMe allrs763195944
SNP Nexus

SNPshotrs763195944
SNPdbers763195944
MSV3drs763195944
GWAS Ctlgrs763195944
Max Magnitude0
ClinVar
Risk rs763195944(C;C)
Alt rs763195944(C;C)
Reference rs763195944(;)
Significance Pathogenic
Disease Precocious puberty
Variation info
Gene MKRN3
CLNDBN Precocious puberty, central, 2
Reversed 0
HGVS NC_000015.9:g.23811411dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000050241.2,