rs63750129

Orientation

plus

Stabilized

plus

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

Make rs63750129(A;C)

Make rs63750129(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

45996612

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750129
dbSNP (classic)	rs63750129
ClinGen	rs63750129
ebi	rs63750129
HLI	rs63750129
Exac	rs63750129
Gnomad	rs63750129
Varsome	rs63750129
LitVar	rs63750129
Map	rs63750129
PheGenI	rs63750129
Biobank	rs63750129
1000 genomes	rs63750129
hgdp	rs63750129
ensembl	rs63750129
geneview	rs63750129
scholar	rs63750129
google	rs63750129
pharmgkb	rs63750129
gwascentral	rs63750129
openSNP	rs63750129
23andMe	rs63750129
SNPshot	rs63750129
SNPdbe	rs63750129
MSV3d	rs63750129
GWAS Ctlg	rs63750129

Max Magnitude

0

OMIM	157140
Desc	Pick's disease
Variant	0015
Related	also

ClinVar
Risk	rs63750129(C;C)
Alt	rs63750129(C;C)
Reference	Rs63750129(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.44073978A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015328.26, RCV000084515.1,