rs63750092

Orientation

plus

Stabilized

plus

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

Make rs63750092(A;T)

Make rs63750092(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46014277

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750092
dbSNP (classic)	rs63750092
ClinGen	rs63750092
ebi	rs63750092
HLI	rs63750092
Exac	rs63750092
Gnomad	rs63750092
Varsome	rs63750092
LitVar	rs63750092
Map	rs63750092
PheGenI	rs63750092
Biobank	rs63750092
1000 genomes	rs63750092
hgdp	rs63750092
ensembl	rs63750092
geneview	rs63750092
scholar	rs63750092
google	rs63750092
pharmgkb	rs63750092
gwascentral	rs63750092
openSNP	rs63750092
23andMe	rs63750092
SNPshot	rs63750092
SNPdbe	rs63750092
MSV3d	rs63750092
GWAS Ctlg	rs63750092

Max Magnitude

0

OMIM	157140
Desc
Variant	0024
Related	also

ClinVar
Risk	rs63750092(T;T)
Alt	rs63750092(T;T)
Reference	Rs63750092(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.44091643A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015338.26, RCV000084543.1,