rs8069834

Orientation

plus

Stabilized

plus

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

Make rs8069834(A;G)

Make rs8069834(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

10394341

Gene	MYH8, MYHAS

is a	snp
is	mentioned by
dbSNP	rs8069834
dbSNP (classic)	rs8069834
ClinGen	rs8069834
ebi	rs8069834
HLI	rs8069834
Exac	rs8069834
Gnomad	rs8069834
Varsome	rs8069834
LitVar	rs8069834
Map	rs8069834
PheGenI	rs8069834
Biobank	rs8069834
1000 genomes	rs8069834
hgdp	rs8069834
ensembl	rs8069834
geneview	rs8069834
scholar	rs8069834
google	rs8069834
pharmgkb	rs8069834
gwascentral	rs8069834
openSNP	rs8069834
23andMe	rs8069834
SNPshot	rs8069834
SNPdbe	rs8069834
MSV3d	rs8069834
GWAS Ctlg	rs8069834

GMAF

0.4959

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs8069834(G;G)
Alt	rs8069834(G;G)
Reference	Rs8069834(A;A)
Significance	Probable-non-pathogenic
Disease	not specified Hecht syndrome
Variation	info
Gene	MYHAS MYH8
CLNDBN	not specified Hecht syndrome
Reversed	0
HGVS	NC_000017.10:g.10297658A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000117692.2, RCV000341726.1,