rs387906885

Orientation

plus

Stabilized

plus

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

Make rs387906885(A;A)

Make rs387906885(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137101607

Gene	LOC101930307, MAN1B1

is a	snp
is	mentioned by
dbSNP	rs387906885
dbSNP (classic)	rs387906885
ClinGen	rs387906885
ebi	rs387906885
HLI	rs387906885
Exac	rs387906885
Gnomad	rs387906885
Varsome	rs387906885
LitVar	rs387906885
Map	rs387906885
PheGenI	rs387906885
Biobank	rs387906885
1000 genomes	rs387906885
hgdp	rs387906885
ensembl	rs387906885
geneview	rs387906885
scholar	rs387906885
google	rs387906885
pharmgkb	rs387906885
gwascentral	rs387906885
openSNP	rs387906885
23andMe	rs387906885
SNPshot	rs387906885
SNPdbe	rs387906885
MSV3d	rs387906885
GWAS Ctlg	rs387906885

Max Magnitude

0

ClinVar
Risk	rs387906885(A;A)
Alt	rs387906885(A;A)
Reference	Rs387906885(G;G)
Significance	Pathogenic
Disease	Mental retardation not provided
Variation	info
Gene	MAN1B1
CLNDBN	Mental retardation, autosomal recessive 15 not provided
Reversed	0
HGVS	NC_000009.11:g.139996059G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023366.2, RCV000487556.1,