rs63750512

Orientation

plus

Stabilized

plus

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

Make rs63750512(A;A)

Make rs63750512(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46024010

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750512
dbSNP (classic)	rs63750512
ClinGen	rs63750512
ebi	rs63750512
HLI	rs63750512
Exac	rs63750512
Gnomad	rs63750512
Varsome	rs63750512
LitVar	rs63750512
Map	rs63750512
PheGenI	rs63750512
Biobank	rs63750512
1000 genomes	rs63750512
hgdp	rs63750512
ensembl	rs63750512
geneview	rs63750512
scholar	rs63750512
google	rs63750512
pharmgkb	rs63750512
gwascentral	rs63750512
openSNP	rs63750512
23andMe	rs63750512
SNPshot	rs63750512
SNPdbe	rs63750512
MSV3d	rs63750512
GWAS Ctlg	rs63750512

Max Magnitude

0

OMIM	157140
Desc	Pick's disease
Variant	0011
Related	also

ClinVar
Risk	rs63750512(A;A) rs63750512(C;C)
Alt	rs63750512(A;A) rs63750512(C;C)
Reference	Rs63750512(G;G)
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.44101376G>A; NC_000017.10:g.44101376G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015324.26, RCV000084553.1,