rs1064796014

Orientation

minus

Stabilized

minus

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

Chromosome

21

Position

36937301

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs1064796014
dbSNP (classic)	rs1064796014
ClinGen	rs1064796014
ebi	rs1064796014
HLI	rs1064796014
Exac	rs1064796014
Gnomad	rs1064796014
Varsome	rs1064796014
LitVar	rs1064796014
Map	rs1064796014
PheGenI	rs1064796014
Biobank	rs1064796014
1000 genomes	rs1064796014
hgdp	rs1064796014
ensembl	rs1064796014
geneview	rs1064796014
scholar	rs1064796014
google	rs1064796014
pharmgkb	rs1064796014
gwascentral	rs1064796014
openSNP	rs1064796014
23andMe	rs1064796014
SNPshot	rs1064796014
SNPdbe	rs1064796014
MSV3d	rs1064796014
GWAS Ctlg	rs1064796014

Max Magnitude

0

ClinVar
Risk	rs1064796014(TTGCTTGAGATTAAGCCTGAGATTAAGG;TTGCTTGAGATTAAGCCTGAGATTAAGG)
Alt	rs1064796014(TTGCTTGAGATTAAGCCTGAGATTAAGG;TTGCTTGAGATTAAGCCTGAGATTAAGG)
Reference	Rs1064796014(CGAAGCCTGAACCTTCT;CGAAGCCTGAACCTTCT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	1
HGVS	NC_000021.8:g.38309601_38309617del17insCCTTAATCTCAGGCTTAATCTCAAGCAA
CLNSRC
CLNACC	RCV000479512.1,