rs3736360

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	0	Likely to be benign according to ClinVar
(G;G)	0	common in clinvar

Make rs3736360(A;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

21823627

Gene	HSPG2, LDLRAD2

is a	snp
is	mentioned by
dbSNP	rs3736360
dbSNP (classic)	rs3736360
ClinGen	rs3736360
ebi	rs3736360
HLI	rs3736360
Exac	rs3736360
Gnomad	rs3736360
Varsome	rs3736360
LitVar	rs3736360
Map	rs3736360
PheGenI	rs3736360
Biobank	rs3736360
1000 genomes	rs3736360
hgdp	rs3736360
ensembl	rs3736360
geneview	rs3736360
scholar	rs3736360
google	rs3736360
pharmgkb	rs3736360
gwascentral	rs3736360
openSNP	rs3736360
23andMe	rs3736360
SNPshot	rs3736360
SNPdbe	rs3736360
MSV3d	rs3736360
GWAS Ctlg	rs3736360

GMAF

0.157

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs3736360(A;A)
Alt	rs3736360(A;A)
Reference	Rs3736360(G;G)
Significance	Non-pathogenic
Disease	Dyssegmental Dysplasia Schwartz Jampel syndrome type 1
Variation	info
Gene	LDLRAD2 HSPG2
CLNDBN	Dyssegmental Dysplasia Schwartz Jampel syndrome type 1
Reversed	1
HGVS	NC_000001.10:g.22150120C>T
CLNSRC
CLNACC	RCV000278239.1, RCV000375072.1,