rs63751165

Orientation

plus

Stabilized

plus

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

Make rs63751165(A;A)

Make rs63751165(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010401

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs63751165
dbSNP (classic)	rs63751165
ClinGen	rs63751165
ebi	rs63751165
HLI	rs63751165
Exac	rs63751165
Gnomad	rs63751165
Varsome	rs63751165
LitVar	rs63751165
Map	rs63751165
PheGenI	rs63751165
Biobank	rs63751165
1000 genomes	rs63751165
hgdp	rs63751165
ensembl	rs63751165
geneview	rs63751165
scholar	rs63751165
google	rs63751165
pharmgkb	rs63751165
gwascentral	rs63751165
openSNP	rs63751165
23andMe	rs63751165
SNPshot	rs63751165
SNPdbe	rs63751165
MSV3d	rs63751165
GWAS Ctlg	rs63751165

Max Magnitude

0

OMIM	157140
Desc
Variant	0010
Related	also

ClinVar
Risk	rs63751165(A;A)
Alt	rs63751165(A;A)
Reference	Rs63751165(G;G)
Significance	Pathogenic
Disease	Frontotemporal dementia not provided
Variation	info
Gene	MAPT
CLNDBN	Frontotemporal dementia not provided
Reversed	0
HGVS	NC_000017.10:g.44087767G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015323.26, RCV000084530.1,