rs63750376

Orientation

plus

Stabilized

plus

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

Make rs63750376(G;T)

Make rs63750376(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

45996657

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750376
dbSNP (classic)	rs63750376
ClinGen	rs63750376
ebi	rs63750376
HLI	rs63750376
Exac	rs63750376
Gnomad	rs63750376
Varsome	rs63750376
LitVar	rs63750376
Map	rs63750376
PheGenI	rs63750376
Biobank	rs63750376
1000 genomes	rs63750376
hgdp	rs63750376
ensembl	rs63750376
geneview	rs63750376
scholar	rs63750376
google	rs63750376
pharmgkb	rs63750376
gwascentral	rs63750376
openSNP	rs63750376
23andMe	rs63750376
SNPshot	rs63750376
SNPdbe	rs63750376
MSV3d	rs63750376
GWAS Ctlg	rs63750376

Max Magnitude

0

OMIM	157140
Desc
Variant	0002
Related	also

ClinVar
Risk	rs63750376(T;T)
Alt	rs63750376(T;T)
Reference	Rs63750376(G;G)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	MAPT
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.44074023G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015315.26, RCV000084519.1,