rs139562274

Orientation

plus

Stabilized

plus

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

Make rs139562274(A;A)

Make rs139562274(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89317389

Gene	FANCI, POLG

is a	snp
is	mentioned by
dbSNP	rs139562274
dbSNP (classic)	rs139562274
ClinGen	rs139562274
ebi	rs139562274
HLI	rs139562274
Exac	rs139562274
Gnomad	rs139562274
Varsome	rs139562274
LitVar	rs139562274
Map	rs139562274
PheGenI	rs139562274
Biobank	rs139562274
1000 genomes	rs139562274
hgdp	rs139562274
ensembl	rs139562274
geneview	rs139562274
scholar	rs139562274
google	rs139562274
pharmgkb	rs139562274
gwascentral	rs139562274
openSNP	rs139562274
23andMe	rs139562274
SNPshot	rs139562274
SNPdbe	rs139562274
MSV3d	rs139562274
GWAS Ctlg	rs139562274

Max Magnitude

0

ClinVar
Risk	rs139562274(A;A) rs139562274(C;C)
Alt	rs139562274(A;A) rs139562274(C;C)
Reference	Rs139562274(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	POLG FANCI
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.89860620G>C
CLNSRC
CLNACC	RCV000188630.1,