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

rs121912519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912519(A;A)
Make rs121912519(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48688084
GeneLHCGR, STON1-GTF2A1L
is asnp
is mentioned by
dbSNPrs121912519
ebirs121912519
HLIrs121912519
Exacrs121912519
Varsomers121912519
Maprs121912519
PheGenIrs121912519
hapmaprs121912519
1000 genomesrs121912519
hgdprs121912519
ensemblrs121912519
gopubmedrs121912519
geneviewrs121912519
scholarrs121912519
googlers121912519
pharmgkbrs121912519
gwascentralrs121912519
openSNPrs121912519
23andMers121912519
23andMe allrs121912519
SNP Nexus

SNPshotrs121912519
SNPdbers121912519
MSV3drs121912519
GWAS Ctlgrs121912519
Max Magnitude0
OMIM152790
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912519(A;A)
Alt rs121912519(A;A)
Reference rs121912519(G;G)
Significance Pathogenic
Disease Gonadotropin-independent familial sexual precocity
Variation info
Gene STON1-GTF2A1L GTF2A1L LHCGR
CLNDBN Gonadotropin-independent familial sexual precocity
Reversed 1
HGVS NC_000002.11:g.48915223C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015462.28,