rs199422218

Merged into

rs63751392

Orientation

plus

Stabilized

plus

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

Make rs199422218(-;-)

Make rs199422218(-;AAT)

Reference

GRCh38 38.1/141

Chromosome

17

Position

46010373

Gene

MAPT

is a	snp
is	mentioned by
dbSNP	rs199422218
dbSNP (classic)	rs199422218
ClinGen	rs199422218
ebi	rs199422218
HLI	rs199422218
Exac	rs199422218
Gnomad	rs199422218
Varsome	rs199422218
LitVar	rs199422218
Map	rs199422218
PheGenI	rs199422218
Biobank	rs199422218
1000 genomes	rs199422218
hgdp	rs199422218
ensembl	rs199422218
geneview	rs199422218
scholar	rs199422218
google	rs199422218
pharmgkb	rs199422218
gwascentral	rs199422218
openSNP	rs199422218
23andMe	rs199422218
SNPshot	rs199422218
SNPdbe	rs199422218
MSV3d	rs199422218
GWAS Ctlg	rs199422218

Status

Merged into rs63751392

Max Magnitude

0

ClinVar
Risk
Alt
Reference	rs199422218(ATA;ATA)
Significance	Other
Disease	Supranuclear palsy Parkinson disease not provided
Variation	info
Gene	MAPT
CLNDBN	Supranuclear palsy, progressive, 1, atypical Parkinson disease, late-onset not provided
Reversed	0
HGVS	NC_000017.10:g.44087740_44087742delATA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015334.26, RCV000015335.3, RCV000084581.1,