rs104893936

Orientation

minus

Stabilized

minus

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

Make rs104893936(A;A)

Make rs104893936(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

176626472

Gene

SNCB

is a	snp
is	mentioned by
dbSNP	rs104893936
dbSNP (classic)	rs104893936
ClinGen	rs104893936
ebi	rs104893936
HLI	rs104893936
Exac	rs104893936
Gnomad	rs104893936
Varsome	rs104893936
LitVar	rs104893936
Map	rs104893936
PheGenI	rs104893936
Biobank	rs104893936
1000 genomes	rs104893936
hgdp	rs104893936
ensembl	rs104893936
geneview	rs104893936
scholar	rs104893936
google	rs104893936
pharmgkb	rs104893936
gwascentral	rs104893936
openSNP	rs104893936
23andMe	rs104893936
SNPshot	rs104893936
SNPdbe	rs104893936
MSV3d	rs104893936
GWAS Ctlg	rs104893936

Max Magnitude

0

OMIM	602569
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893936(A;A) rs104893936(C;C)
Alt	rs104893936(A;A) rs104893936(C;C)
Reference	Rs104893936(G;G)
Significance	Pathogenic
Disease	Lewy body dementia
Variation	info
Gene	SNCB
CLNDBN	Lewy body dementia
Reversed	1
HGVS	NC_000005.9:g.176053473C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007440.2,