rs149733264

Orientation

plus

Stabilized

plus

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

Make rs149733264(C;C)

Make rs149733264(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

21

Position

36754358

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs149733264
dbSNP (classic)	rs149733264
ClinGen	rs149733264
ebi	rs149733264
HLI	rs149733264
Exac	rs149733264
Gnomad	rs149733264
Varsome	rs149733264
LitVar	rs149733264
Map	rs149733264
PheGenI	rs149733264
Biobank	rs149733264
1000 genomes	rs149733264
hgdp	rs149733264
ensembl	rs149733264
geneview	rs149733264
scholar	rs149733264
google	rs149733264
pharmgkb	rs149733264
gwascentral	rs149733264
openSNP	rs149733264
23andMe	rs149733264
SNPshot	rs149733264
SNPdbe	rs149733264
MSV3d	rs149733264
GWAS Ctlg	rs149733264

Max Magnitude

0

ClinVar
Risk	rs149733264(C;C)
Alt	rs149733264(C;C)
Reference	Rs149733264(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.38126659T>A
CLNSRC
CLNACC	RCV000185964.1,