rs63750711

Orientation

plus

Stabilized

plus

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

Make rs63750711(A;T)

Make rs63750711(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46018645

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750711
dbSNP (classic)	rs63750711
ClinGen	rs63750711
ebi	rs63750711
HLI	rs63750711
Exac	rs63750711
Gnomad	rs63750711
Varsome	rs63750711
LitVar	rs63750711
Map	rs63750711
PheGenI	rs63750711
Biobank	rs63750711
1000 genomes	rs63750711
hgdp	rs63750711
ensembl	rs63750711
geneview	rs63750711
scholar	rs63750711
google	rs63750711
pharmgkb	rs63750711
gwascentral	rs63750711
openSNP	rs63750711
23andMe	rs63750711
SNPshot	rs63750711
SNPdbe	rs63750711
MSV3d	rs63750711
GWAS Ctlg	rs63750711

Max Magnitude

0

OMIM	157140
Desc
Variant	0014
Related	also

ClinVar
Risk	rs63750711(T;T)
Alt	rs63750711(T;T)
Reference	Rs63750711(A;A)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	MAPT
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.44096011A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015327.27, RCV000084549.1,