rs374156844

Orientation

plus

Stabilized

plus

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

Make rs374156844(A;A)

Make rs374156844(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

33177700

Gene

COL11A2

is a	snp
is	mentioned by
dbSNP	rs374156844
dbSNP (classic)	rs374156844
ClinGen	rs374156844
ebi	rs374156844
HLI	rs374156844
Exac	rs374156844
Gnomad	rs374156844
Varsome	rs374156844
LitVar	rs374156844
Map	rs374156844
PheGenI	rs374156844
Biobank	rs374156844
1000 genomes	rs374156844
hgdp	rs374156844
ensembl	rs374156844
geneview	rs374156844
scholar	rs374156844
google	rs374156844
pharmgkb	rs374156844
gwascentral	rs374156844
openSNP	rs374156844
23andMe	rs374156844
SNPshot	rs374156844
SNPdbe	rs374156844
MSV3d	rs374156844
GWAS Ctlg	rs374156844

Max Magnitude

0

ClinVar
Risk	rs374156844(A;A)
Alt	rs374156844(A;A)
Reference	Rs374156844(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COL11A2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.33145477G>A
CLNSRC
CLNACC	RCV000487615.1,