rs587776966

Orientation

plus

Stabilized

plus

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

Make rs587776966(A;A)

Make rs587776966(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

123083100

Gene

CLMP

is a	snp
is	mentioned by
dbSNP	rs587776966
dbSNP (classic)	rs587776966
ClinGen	rs587776966
ebi	rs587776966
HLI	rs587776966
Exac	rs587776966
Gnomad	rs587776966
Varsome	rs587776966
LitVar	rs587776966
Map	rs587776966
PheGenI	rs587776966
Biobank	rs587776966
1000 genomes	rs587776966
hgdp	rs587776966
ensembl	rs587776966
geneview	rs587776966
scholar	rs587776966
google	rs587776966
pharmgkb	rs587776966
gwascentral	rs587776966
openSNP	rs587776966
23andMe	rs587776966
SNPshot	rs587776966
SNPdbe	rs587776966
MSV3d	rs587776966
GWAS Ctlg	rs587776966

Max Magnitude

0

ClinVar
Risk	rs587776966(A;A)
Alt	rs587776966(A;A)
Reference	Rs587776966(G;G)
Significance	Pathogenic
Disease	Congenital short bowel syndrome
Variation	info
Gene	CLMP
CLNDBN	Congenital short bowel syndrome
Reversed	0
HGVS	NC_000011.9:g.122953808G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043526.5,