rs148981273

Orientation

plus

Stabilized

plus

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

Make rs148981273(C;T)

Make rs148981273(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

36938880

Gene

HLCS

is a	snp
is	mentioned by
dbSNP	rs148981273
dbSNP (classic)	rs148981273
ClinGen	rs148981273
ebi	rs148981273
HLI	rs148981273
Exac	rs148981273
Gnomad	rs148981273
Varsome	rs148981273
LitVar	rs148981273
Map	rs148981273
PheGenI	rs148981273
Biobank	rs148981273
1000 genomes	rs148981273
hgdp	rs148981273
ensembl	rs148981273
geneview	rs148981273
scholar	rs148981273
google	rs148981273
pharmgkb	rs148981273
gwascentral	rs148981273
openSNP	rs148981273
23andMe	rs148981273
SNPshot	rs148981273
SNPdbe	rs148981273
MSV3d	rs148981273
GWAS Ctlg	rs148981273

Max Magnitude

0

ClinVar
Risk	rs148981273(T;T)
Alt	rs148981273(T;T)
Reference	Rs148981273(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HLCS
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.38311180C>T
CLNSRC
CLNACC	RCV000487407.1,