rs786205608

Orientation

plus

Stabilized

plus

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

Make rs786205608(A;G)

Make rs786205608(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

93787842

Gene

TMEM67

is a	snp
is	mentioned by
dbSNP	rs786205608
dbSNP (classic)	rs786205608
ClinGen	rs786205608
ebi	rs786205608
HLI	rs786205608
Exac	rs786205608
Gnomad	rs786205608
Varsome	rs786205608
LitVar	rs786205608
Map	rs786205608
PheGenI	rs786205608
Biobank	rs786205608
1000 genomes	rs786205608
hgdp	rs786205608
ensembl	rs786205608
geneview	rs786205608
scholar	rs786205608
google	rs786205608
pharmgkb	rs786205608
gwascentral	rs786205608
openSNP	rs786205608
23andMe	rs786205608
SNPshot	rs786205608
SNPdbe	rs786205608
MSV3d	rs786205608
GWAS Ctlg	rs786205608

Max Magnitude

0

ClinVar
Risk	rs786205608(G;G)
Alt	rs786205608(G;G)
Reference	Rs786205608(A;A)
Significance	Other
Disease	not provided
Variation	info
Gene	TMEM67
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.94800070A>G
CLNSRC
CLNACC	RCV000171449.2,