rs386833512

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs386833512(A;A)

Make rs386833512(A;C)

Reference

GRCh38.p7 38.3/151

Chromosome

2

Position

48963061

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs386833512
dbSNP (classic)	rs386833512
ClinGen	rs386833512
ebi	rs386833512
HLI	rs386833512
Exac	rs386833512
Gnomad	rs386833512
Varsome	rs386833512
LitVar	rs386833512
Map	rs386833512
PheGenI	rs386833512
Biobank	rs386833512
1000 genomes	rs386833512
hgdp	rs386833512
ensembl	rs386833512
geneview	rs386833512
scholar	rs386833512
google	rs386833512
pharmgkb	rs386833512
gwascentral	rs386833512
openSNP	rs386833512
23andMe	rs386833512
SNPshot	rs386833512
SNPdbe	rs386833512
MSV3d	rs386833512
GWAS Ctlg	rs386833512

Max Magnitude

0

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

OMIM pathogenic variant