rs121912644

Orientation

plus

Stabilized

plus

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

Make rs121912644(A;A)

Make rs121912644(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

180274568

Gene	ACBD6, LHX4, LHX4-AS1

is a	snp
is	mentioned by
dbSNP	rs121912644
dbSNP (classic)	rs121912644
ClinGen	rs121912644
ebi	rs121912644
HLI	rs121912644
Exac	rs121912644
Gnomad	rs121912644
Varsome	rs121912644
LitVar	rs121912644
Map	rs121912644
PheGenI	rs121912644
Biobank	rs121912644
1000 genomes	rs121912644
hgdp	rs121912644
ensembl	rs121912644
geneview	rs121912644
scholar	rs121912644
google	rs121912644
pharmgkb	rs121912644
gwascentral	rs121912644
openSNP	rs121912644
23andMe	rs121912644
SNPshot	rs121912644
SNPdbe	rs121912644
MSV3d	rs121912644
GWAS Ctlg	rs121912644

Max Magnitude

0

OMIM	602146
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121912644(A;A)
Alt	rs121912644(A;A)
Reference	Rs121912644(C;C)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	LHX4 LHX4-AS1
CLNDBN	Pituitary hormone deficiency, combined 4
Reversed	0
HGVS	NC_000001.10:g.180243703C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007939.2,