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rs386833512

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common genotype
Make rs386833512(A;A)
Make rs386833512(A;C)
ReferenceGRCh38.p7 38.3/151
Chromosome2
Position48963061
GeneFSHR
is asnp
is mentioned by
dbSNPrs386833512
dbSNP (classic)rs386833512
ClinGenrs386833512
ebirs386833512
HLIrs386833512
Exacrs386833512
Gnomadrs386833512
Varsomers386833512
LitVarrs386833512
Maprs386833512
PheGenIrs386833512
Biobankrs386833512
1000 genomesrs386833512
hgdprs386833512
ensemblrs386833512
geneviewrs386833512
scholarrs386833512
googlers386833512
pharmgkbrs386833512
gwascentralrs386833512
openSNPrs386833512
23andMers386833512
SNPshotrs386833512
SNPdbers386833512
MSV3drs386833512
GWAS Ctlgrs386833512
Max Magnitude0

aka NM_000145.3(FSHR):c.1760C>A or (p.Pro587His)

OMIM pathogenic variant