rs796051978

Orientation

minus

Stabilized

minus

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

Make rs796051978(-;-)

Make rs796051978(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

21

Position

36756660

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs796051978
dbSNP (classic)	rs796051978
ClinGen	rs796051978
ebi	rs796051978
HLI	rs796051978
Exac	rs796051978
Gnomad	rs796051978
Varsome	rs796051978
LitVar	rs796051978
Map	rs796051978
PheGenI	rs796051978
Biobank	rs796051978
1000 genomes	rs796051978
hgdp	rs796051978
ensembl	rs796051978
geneview	rs796051978
scholar	rs796051978
google	rs796051978
pharmgkb	rs796051978
gwascentral	rs796051978
openSNP	rs796051978
23andMe	rs796051978
SNPshot	rs796051978
SNPdbe	rs796051978
MSV3d	rs796051978
GWAS Ctlg	rs796051978

Max Magnitude

0

ClinVar
Risk	rs796051978(-;-)
Alt	rs796051978(-;-)
Reference	Rs796051978(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	1
HGVS	NC_000021.8:g.38128961delA
CLNSRC
CLNACC	RCV000185967.1,