rs8042919

plus

Geno	Mag	Summary
(G;G)	0	common on affy axiom data

Make rs8042919(A;A)

Make rs8042919(A;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

50586433

Gene

TRPM7

is a	snp
is	mentioned by
dbSNP	rs8042919
dbSNP (classic)	rs8042919
ClinGen	rs8042919
ebi	rs8042919
HLI	rs8042919
Exac	rs8042919
Gnomad	rs8042919
Varsome	rs8042919
LitVar	rs8042919
Map	rs8042919
PheGenI	rs8042919
Biobank	rs8042919
1000 genomes	rs8042919
hgdp	rs8042919
ensembl	rs8042919
geneview	rs8042919
scholar	rs8042919
google	rs8042919
pharmgkb	rs8042919
gwascentral	rs8042919
openSNP	rs8042919
23andMe	rs8042919
SNPshot	rs8042919
SNPdbe	rs8042919
MSV3d	rs8042919
GWAS Ctlg	rs8042919

GMAF

0.07071

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 19405049] TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of Japan

OMIM	605692
Desc	TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 7;
Variant
Related	also

OMIM	605692
Desc
Variant	0001
Related	also

ClinVar
Risk	rs8042919(A;A)
Alt	rs8042919(A;A)
Reference	Rs8042919(G;G)
Significance	Other
Disease	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
Variation	info
Gene	TRPM7
CLNDBN	Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1, susceptibility to
Reversed	0
HGVS	NC_000015.9:g.50878630G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005076.4,

[PMID 19149903 ] Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women.

[PMID 19268276 ] Genome-wide association study of smoking initiation and current smoking.

[PMID 24952306 ] The association between single-nucleotide polymorphisms of TRPM7 gene and breast cancer in Han Population of Northeast China