rs63750972

Orientation

plus

Stabilized

plus

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

Make rs63750972(C;T)

Make rs63750972(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010416

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750972
dbSNP (classic)	rs63750972
ClinGen	rs63750972
ebi	rs63750972
HLI	rs63750972
Exac	rs63750972
Gnomad	rs63750972
Varsome	rs63750972
LitVar	rs63750972
Map	rs63750972
PheGenI	rs63750972
Biobank	rs63750972
1000 genomes	rs63750972
hgdp	rs63750972
ensembl	rs63750972
geneview	rs63750972
scholar	rs63750972
google	rs63750972
pharmgkb	rs63750972
gwascentral	rs63750972
openSNP	rs63750972
23andMe	rs63750972
SNPshot	rs63750972
SNPdbe	rs63750972
MSV3d	rs63750972
GWAS Ctlg	rs63750972

Max Magnitude

0

ClinVar
Risk	rs63750972(T;T)
Alt	rs63750972(T;T)
Reference	Rs63750972(C;C)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	MAPT
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.44087782C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015317.25, RCV000084536.1,