rs786205631

Orientation

plus

Stabilized

plus

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

Make rs786205631(C;C)

Make rs786205631(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

3603614

Gene

COLEC11

is a	snp
is	mentioned by
dbSNP	rs786205631
dbSNP (classic)	rs786205631
ClinGen	rs786205631
ebi	rs786205631
HLI	rs786205631
Exac	rs786205631
Gnomad	rs786205631
Varsome	rs786205631
LitVar	rs786205631
Map	rs786205631
PheGenI	rs786205631
Biobank	rs786205631
1000 genomes	rs786205631
hgdp	rs786205631
ensembl	rs786205631
geneview	rs786205631
scholar	rs786205631
google	rs786205631
pharmgkb	rs786205631
gwascentral	rs786205631
openSNP	rs786205631
23andMe	rs786205631
SNPshot	rs786205631
SNPdbe	rs786205631
MSV3d	rs786205631
GWAS Ctlg	rs786205631

Max Magnitude

0

ClinVar
Risk	rs786205631(C;C)
Alt	rs786205631(C;C)
Reference	Rs786205631(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	COLEC11
CLNDBN	not specified
Reversed	0
HGVS	NC_000002.11:g.3651204G>C
CLNSRC
CLNACC	RCV000171491.2,