rs774610098

Orientation

plus

Stabilized

plus

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

Make rs774610098(A;G)

Make rs774610098(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89327317

Gene	MIR6766, POLG

is a	snp
is	mentioned by
dbSNP	rs774610098
dbSNP (classic)	rs774610098
ClinGen	rs774610098
ebi	rs774610098
HLI	rs774610098
Exac	rs774610098
Gnomad	rs774610098
Varsome	rs774610098
LitVar	rs774610098
Map	rs774610098
PheGenI	rs774610098
Biobank	rs774610098
1000 genomes	rs774610098
hgdp	rs774610098
ensembl	rs774610098
geneview	rs774610098
scholar	rs774610098
google	rs774610098
pharmgkb	rs774610098
gwascentral	rs774610098
openSNP	rs774610098
23andMe	rs774610098
SNPshot	rs774610098
SNPdbe	rs774610098
MSV3d	rs774610098
GWAS Ctlg	rs774610098

Max Magnitude

0

ClinVar
Risk	rs774610098(G;G)
Alt	rs774610098(G;G)
Reference	Rs774610098(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MIR6766 POLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.89870548A>G
CLNSRC
CLNACC	RCV000188653.1,