rs63750869

Orientation

plus

Stabilized

plus

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

Make rs63750869(A;A)

Make rs63750869(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

46018707

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63750869
dbSNP (classic)	rs63750869
ClinGen	rs63750869
ebi	rs63750869
HLI	rs63750869
Exac	rs63750869
Gnomad	rs63750869
Varsome	rs63750869
LitVar	rs63750869
Map	rs63750869
PheGenI	rs63750869
Biobank	rs63750869
1000 genomes	rs63750869
hgdp	rs63750869
ensembl	rs63750869
geneview	rs63750869
scholar	rs63750869
google	rs63750869
pharmgkb	rs63750869
gwascentral	rs63750869
openSNP	rs63750869
23andMe	rs63750869
SNPshot	rs63750869
SNPdbe	rs63750869
MSV3d	rs63750869
GWAS Ctlg	rs63750869

Max Magnitude

0

ClinVar
Risk	rs63750869(A;A)
Alt	rs63750869(A;A)
Reference	Rs63750869(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAPT
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.44096073G>A
CLNSRC
CLNACC	RCV000084551.1,