rs772791252

Orientation

plus

Stabilized

plus

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

Make rs772791252(A;A)

Make rs772791252(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

36759829

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs772791252
dbSNP (classic)	rs772791252
ClinGen	rs772791252
ebi	rs772791252
HLI	rs772791252
Exac	rs772791252
Gnomad	rs772791252
Varsome	rs772791252
LitVar	rs772791252
Map	rs772791252
PheGenI	rs772791252
Biobank	rs772791252
1000 genomes	rs772791252
hgdp	rs772791252
ensembl	rs772791252
geneview	rs772791252
scholar	rs772791252
google	rs772791252
pharmgkb	rs772791252
gwascentral	rs772791252
openSNP	rs772791252
23andMe	rs772791252
SNPshot	rs772791252
SNPdbe	rs772791252
MSV3d	rs772791252
GWAS Ctlg	rs772791252

Max Magnitude

0

ClinVar
Risk	rs772791252(A;A)
Alt	rs772791252(A;A)
Reference	Rs772791252(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.38132130G>A
CLNSRC
CLNACC	RCV000489166.1,