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

rs5030646

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs5030646(-;-)
Make rs5030646(-;TG)
Make rs5030646(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position30233646
GeneFSHB, LOC105376607
is asnp
is mentioned by
dbSNPrs5030646
ebirs5030646
HLIrs5030646
Exacrs5030646
Varsomers5030646
Maprs5030646
PheGenIrs5030646
hapmaprs5030646
1000 genomesrs5030646
hgdprs5030646
ensemblrs5030646
gopubmedrs5030646
geneviewrs5030646
scholarrs5030646
googlers5030646
pharmgkbrs5030646
gwascentralrs5030646
openSNPrs5030646
23andMers5030646
23andMe allrs5030646
SNP Nexus

SNPshotrs5030646
SNPdbers5030646
MSV3drs5030646
GWAS Ctlgrs5030646
Max Magnitude0
ClinVar
Risk rs5030646(;)
Alt rs5030646(;)
Reference rs5030646(GT;GT)
Significance Pathogenic
Disease Follicle-stimulating hormone deficiency
Variation info
Gene FSHB
CLNDBN Follicle-stimulating hormone deficiency, isolated
Reversed 0
HGVS NC_000011.9:g.30255193_30255194delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000017627.29,