rs63751438

Orientation

plus

Stabilized

plus

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

Make rs63751438(C;T)

Make rs63751438(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010388

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63751438
dbSNP (classic)	rs63751438
ClinGen	rs63751438
ebi	rs63751438
HLI	rs63751438
Exac	rs63751438
Gnomad	rs63751438
Varsome	rs63751438
LitVar	rs63751438
Map	rs63751438
PheGenI	rs63751438
Biobank	rs63751438
1000 genomes	rs63751438
hgdp	rs63751438
ensembl	rs63751438
geneview	rs63751438
scholar	rs63751438
google	rs63751438
pharmgkb	rs63751438
gwascentral	rs63751438
openSNP	rs63751438
23andMe	rs63751438
SNPshot	rs63751438
SNPdbe	rs63751438
MSV3d	rs63751438
GWAS Ctlg	rs63751438

Max Magnitude

0

OMIM	157140
Desc
Variant	0012
Related	also

ClinVar
Risk	rs63751438(T;T)
Alt	rs63751438(T;T)
Reference	Rs63751438(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.44087754C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015325.22, RCV000084526.1,