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rs200639521

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs200639521(A;G)
Make rs200639521(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position48725674
GeneLHCGR, STON1-GTF2A1L
is asnp
is mentioned by
dbSNPrs200639521
dbSNP (classic)rs200639521
ClinGenrs200639521
ebirs200639521
HLIrs200639521
Exacrs200639521
Gnomadrs200639521
Varsomers200639521
LitVarrs200639521
Maprs200639521
PheGenIrs200639521
Biobankrs200639521
1000 genomesrs200639521
hgdprs200639521
ensemblrs200639521
geneviewrs200639521
scholarrs200639521
googlers200639521
pharmgkbrs200639521
gwascentralrs200639521
openSNPrs200639521
23andMers200639521
23andMe allrs200639521
SNPshotrs200639521
SNPdbers200639521
MSV3drs200639521
GWAS Ctlgrs200639521
Max Magnitude0
ClinVar
Risk rs200639521(G;G)
Alt rs200639521(G;G)
Reference Rs200639521(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene STON1-GTF2A1L GTF2A1L LHCGR
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48952813A>G
CLNSRC
CLNACC RCV000480873.1,