rs146448211

Orientation

plus

Stabilized

plus

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

Make rs146448211(A;A)

Make rs146448211(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

21

Position

36756558

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs146448211
dbSNP (classic)	rs146448211
ClinGen	rs146448211
ebi	rs146448211
HLI	rs146448211
Exac	rs146448211
Gnomad	rs146448211
Varsome	rs146448211
LitVar	rs146448211
Map	rs146448211
PheGenI	rs146448211
Biobank	rs146448211
1000 genomes	rs146448211
hgdp	rs146448211
ensembl	rs146448211
geneview	rs146448211
scholar	rs146448211
google	rs146448211
pharmgkb	rs146448211
gwascentral	rs146448211
openSNP	rs146448211
23andMe	rs146448211
SNPshot	rs146448211
SNPdbe	rs146448211
MSV3d	rs146448211
GWAS Ctlg	rs146448211

Max Magnitude

0

ClinVar
Risk	rs146448211(A;A)
Alt	rs146448211(A;A)
Reference	Rs146448211(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.38128859G>A
CLNSRC
CLNACC	RCV000185962.1,