rs121908055

Orientation

minus

Stabilized

minus

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

Make rs121908055(A;A)

Make rs121908055(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

67942967

Gene

LCAT

is a	snp
is	mentioned by
dbSNP	rs121908055
dbSNP (classic)	rs121908055
ClinGen	rs121908055
ebi	rs121908055
HLI	rs121908055
Exac	rs121908055
Gnomad	rs121908055
Varsome	rs121908055
LitVar	rs121908055
Map	rs121908055
PheGenI	rs121908055
Biobank	rs121908055
1000 genomes	rs121908055
hgdp	rs121908055
ensembl	rs121908055
geneview	rs121908055
scholar	rs121908055
google	rs121908055
pharmgkb	rs121908055
gwascentral	rs121908055
openSNP	rs121908055
23andMe	rs121908055
SNPshot	rs121908055
SNPdbe	rs121908055
MSV3d	rs121908055
GWAS Ctlg	rs121908055

Max Magnitude

0

OMIM	606967
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121908055(A;A)
Alt	rs121908055(A;A)
Reference	Rs121908055(C;C)
Significance	Pathogenic
Disease	Norum disease
Variation	info
Gene	LCAT
CLNDBN	Norum disease
Reversed	1
HGVS	NC_000016.9:g.67976870G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003856.3,