rs786204823

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CACCCCATC;CACCCCATC)	0	common in clinvar

Make rs786204823(-;-)

Make rs786204823(-;CACCCCATC)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

49016634

Gene

LHB

is a	snp
is	mentioned by
dbSNP	rs786204823
dbSNP (classic)	rs786204823
ClinGen	rs786204823
ebi	rs786204823
HLI	rs786204823
Exac	rs786204823
Gnomad	rs786204823
Varsome	rs786204823
LitVar	rs786204823
Map	rs786204823
PheGenI	rs786204823
Biobank	rs786204823
1000 genomes	rs786204823
hgdp	rs786204823
ensembl	rs786204823
geneview	rs786204823
scholar	rs786204823
google	rs786204823
pharmgkb	rs786204823
gwascentral	rs786204823
openSNP	rs786204823
23andMe	rs786204823
SNPshot	rs786204823
SNPdbe	rs786204823
MSV3d	rs786204823
GWAS Ctlg	rs786204823

Max Magnitude

0

ClinVar
Risk	rs786204823(-;-)
Alt	rs786204823(-;-)
Reference	Rs786204823(CACCCCATC;CACCCCATC)
Significance	Pathogenic
Disease	Isolated lutropin deficiency
Variation	info
Gene	LHB
CLNDBN	Isolated lutropin deficiency
Reversed	1
HGVS	NC_000019.9:g.49519891_49519899delGATGGGGTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000169725.4,