rs63751264

Orientation

plus

Stabilized

plus

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

Make rs63751264(A;T)

Make rs63751264(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46018726

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63751264
dbSNP (classic)	rs63751264
ClinGen	rs63751264
ebi	rs63751264
HLI	rs63751264
Exac	rs63751264
Gnomad	rs63751264
Varsome	rs63751264
LitVar	rs63751264
Map	rs63751264
PheGenI	rs63751264
Biobank	rs63751264
1000 genomes	rs63751264
hgdp	rs63751264
ensembl	rs63751264
geneview	rs63751264
scholar	rs63751264
google	rs63751264
pharmgkb	rs63751264
gwascentral	rs63751264
openSNP	rs63751264
23andMe	rs63751264
SNPshot	rs63751264
SNPdbe	rs63751264
MSV3d	rs63751264
GWAS Ctlg	rs63751264

Max Magnitude

0

OMIM	157140
Desc	Pick's disease
Variant	0016
Related	also

ClinVar
Risk	rs63751264(T;T)
Alt	rs63751264(T;T)
Reference	Rs63751264(A;A)
Significance	Pathogenic
Disease	Pick's disease not provided
Variation	info
Gene	MAPT
CLNDBN	Pick's disease not provided
Reversed	0
HGVS	NC_000017.10:g.44096092A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015329.21, RCV000084552.1,