rs63750756

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs63750756(G;G)

Make rs63750756(G;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010324

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750756
dbSNP (classic)	rs63750756
ClinGen	rs63750756
ebi	rs63750756
HLI	rs63750756
Exac	rs63750756
Gnomad	rs63750756
Varsome	rs63750756
LitVar	rs63750756
Map	rs63750756
PheGenI	rs63750756
Biobank	rs63750756
1000 genomes	rs63750756
hgdp	rs63750756
ensembl	rs63750756
geneview	rs63750756
scholar	rs63750756
google	rs63750756
pharmgkb	rs63750756
gwascentral	rs63750756
openSNP	rs63750756
23andMe	rs63750756
SNPshot	rs63750756
SNPdbe	rs63750756
MSV3d	rs63750756
GWAS Ctlg	rs63750756

Max Magnitude

0

OMIM	157140
Desc
Variant	0009
Related	also

ClinVar
Risk	rs63750756(G;G)
Alt	rs63750756(G;G)
Reference	Rs63750756(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.44087690T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015322.21, RCV000084521.1,