rs267607211

Orientation

minus

Stabilized

minus

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

Make rs267607211(C;C)

Make rs267607211(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

67942686

Gene

LCAT

is a	snp
is	mentioned by
dbSNP	rs267607211
dbSNP (classic)	rs267607211
ClinGen	rs267607211
ebi	rs267607211
HLI	rs267607211
Exac	rs267607211
Gnomad	rs267607211
Varsome	rs267607211
LitVar	rs267607211
Map	rs267607211
PheGenI	rs267607211
Biobank	rs267607211
1000 genomes	rs267607211
hgdp	rs267607211
ensembl	rs267607211
geneview	rs267607211
scholar	rs267607211
google	rs267607211
pharmgkb	rs267607211
gwascentral	rs267607211
openSNP	rs267607211
23andMe	rs267607211
SNPshot	rs267607211
SNPdbe	rs267607211
MSV3d	rs267607211
GWAS Ctlg	rs267607211

Max Magnitude

0

ClinVar
Risk	rs267607211(C;C)
Alt	rs267607211(C;C)
Reference	Rs267607211(T;T)
Significance	Pathogenic
Disease	Norum disease
Variation	info
Gene	LCAT
CLNDBN	Norum disease
Reversed	1
HGVS	NC_000016.9:g.67976589A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003841.3,