rs63750355

Orientation

plus

Stabilized

plus

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

Make rs63750355(C;T)

Make rs63750355(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87253472

Gene

CHMP2B

is a	snp
is	mentioned by
dbSNP	rs63750355
dbSNP (classic)	rs63750355
ClinGen	rs63750355
ebi	rs63750355
HLI	rs63750355
Exac	rs63750355
Gnomad	rs63750355
Varsome	rs63750355
LitVar	rs63750355
Map	rs63750355
PheGenI	rs63750355
Biobank	rs63750355
1000 genomes	rs63750355
hgdp	rs63750355
ensembl	rs63750355
geneview	rs63750355
scholar	rs63750355
google	rs63750355
pharmgkb	rs63750355
gwascentral	rs63750355
openSNP	rs63750355
23andMe	rs63750355
SNPshot	rs63750355
SNPdbe	rs63750355
MSV3d	rs63750355
GWAS Ctlg	rs63750355

Max Magnitude

0

OMIM	609512
Desc
Variant	0004
Related	also

ClinVar
Risk	rs63750355(T;T)
Alt	rs63750355(T;T)
Reference	Rs63750355(C;C)
Significance	Pathogenic
Disease	Frontotemporal Dementia not provided
Variation	info
Gene	CHMP2B
CLNDBN	Frontotemporal Dementia, Chromosome 3-Linked not provided
Reversed	0
HGVS	NC_000003.11:g.87302622C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001722.2, RCV000084276.1,