rs786205601

Orientation

plus

Stabilized

plus

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

Make rs786205601(A;A)

Make rs786205601(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

137717151

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs786205601
dbSNP (classic)	rs786205601
ClinGen	rs786205601
ebi	rs786205601
HLI	rs786205601
Exac	rs786205601
Gnomad	rs786205601
Varsome	rs786205601
LitVar	rs786205601
Map	rs786205601
PheGenI	rs786205601
Biobank	rs786205601
1000 genomes	rs786205601
hgdp	rs786205601
ensembl	rs786205601
geneview	rs786205601
scholar	rs786205601
google	rs786205601
pharmgkb	rs786205601
gwascentral	rs786205601
openSNP	rs786205601
23andMe	rs786205601
SNPshot	rs786205601
SNPdbe	rs786205601
MSV3d	rs786205601
GWAS Ctlg	rs786205601

Max Magnitude

0

ClinVar
Risk	rs786205601(A;A)
Alt	rs786205601(A;A)
Reference	Rs786205601(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EHMT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.140611603G>A
CLNSRC
CLNACC	RCV000171430.1,