rs267607102

Orientation

plus

Stabilized

plus

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

Make rs267607102(A;G)

Make rs267607102(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

11022196

Gene

TARDBP

is a	snp
is	mentioned by
dbSNP	rs267607102
dbSNP (classic)	rs267607102
ClinGen	rs267607102
ebi	rs267607102
HLI	rs267607102
Exac	rs267607102
Gnomad	rs267607102
Varsome	rs267607102
LitVar	rs267607102
Map	rs267607102
PheGenI	rs267607102
Biobank	rs267607102
1000 genomes	rs267607102
hgdp	rs267607102
ensembl	rs267607102
geneview	rs267607102
scholar	rs267607102
google	rs267607102
pharmgkb	rs267607102
gwascentral	rs267607102
openSNP	rs267607102
23andMe	rs267607102
SNPshot	rs267607102
SNPdbe	rs267607102
MSV3d	rs267607102
GWAS Ctlg	rs267607102

Max Magnitude

0

ClinVar
Risk	rs267607102(G;G)
Alt	rs267607102(G;G)
Reference	Rs267607102(A;A)
Significance	Pathogenic
Disease	FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS
Variation	info
Gene	TARDBP
CLNDBN	FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
Reversed	0
HGVS	NC_000001.10:g.11082253A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005549.3,