rs63750570

Orientation

plus

Stabilized

plus

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

Make rs63750570(A;A)

Make rs63750570(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46018629

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750570
dbSNP (classic)	rs63750570
ClinGen	rs63750570
ebi	rs63750570
HLI	rs63750570
Exac	rs63750570
Gnomad	rs63750570
Varsome	rs63750570
LitVar	rs63750570
Map	rs63750570
PheGenI	rs63750570
Biobank	rs63750570
1000 genomes	rs63750570
hgdp	rs63750570
ensembl	rs63750570
geneview	rs63750570
scholar	rs63750570
google	rs63750570
pharmgkb	rs63750570
gwascentral	rs63750570
openSNP	rs63750570
23andMe	rs63750570
SNPshot	rs63750570
SNPdbe	rs63750570
MSV3d	rs63750570
GWAS Ctlg	rs63750570

Max Magnitude

0

OMIM	157140
Desc
Variant	0008
Related	also

ClinVar
Risk	rs63750570(A;A)
Alt	rs63750570(A;A)
Reference	Rs63750570(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.44095995G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015321.25, RCV000084548.1,