rs63750912

Orientation

plus

Stabilized

plus

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

Make rs63750912(C;C)

Make rs63750912(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010375

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750912
dbSNP (classic)	rs63750912
ClinGen	rs63750912
ebi	rs63750912
HLI	rs63750912
Exac	rs63750912
Gnomad	rs63750912
Varsome	rs63750912
LitVar	rs63750912
Map	rs63750912
PheGenI	rs63750912
Biobank	rs63750912
1000 genomes	rs63750912
hgdp	rs63750912
ensembl	rs63750912
geneview	rs63750912
scholar	rs63750912
google	rs63750912
pharmgkb	rs63750912
gwascentral	rs63750912
openSNP	rs63750912
23andMe	rs63750912
SNPshot	rs63750912
SNPdbe	rs63750912
MSV3d	rs63750912
GWAS Ctlg	rs63750912

Max Magnitude

0

OMIM	157140
Desc
Variant	0013
Related	also

ClinVar
Risk	rs63750912(C;C)
Alt	rs63750912(C;C)
Reference	Rs63750912(T;T)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	MAPT
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.44087741T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015326.22, RCV000084525.1,