rs369634007

Orientation

plus

Stabilized

plus

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

Make rs369634007(A;G)

Make rs369634007(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

112098688

Gene

TMEM87B

is a	snp
is	mentioned by
dbSNP	rs369634007
dbSNP (classic)	rs369634007
ClinGen	rs369634007
ebi	rs369634007
HLI	rs369634007
Exac	rs369634007
Gnomad	rs369634007
Varsome	rs369634007
LitVar	rs369634007
Map	rs369634007
PheGenI	rs369634007
Biobank	rs369634007
1000 genomes	rs369634007
hgdp	rs369634007
ensembl	rs369634007
geneview	rs369634007
scholar	rs369634007
google	rs369634007
pharmgkb	rs369634007
gwascentral	rs369634007
openSNP	rs369634007
23andMe	rs369634007
SNPshot	rs369634007
SNPdbe	rs369634007
MSV3d	rs369634007
GWAS Ctlg	rs369634007

Max Magnitude

0

ClinVar
Risk	rs369634007(G;G)
Alt	rs369634007(G;G)
Reference	Rs369634007(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TMEM87B
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.112856265A>G
CLNSRC
CLNACC	RCV000208660.1,