rs1064796074

Orientation

minus

Stabilized

minus

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

Chromosome

9

Position

95150014

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1064796074
dbSNP (classic)	rs1064796074
ClinGen	rs1064796074
ebi	rs1064796074
HLI	rs1064796074
Exac	rs1064796074
Gnomad	rs1064796074
Varsome	rs1064796074
LitVar	rs1064796074
Map	rs1064796074
PheGenI	rs1064796074
Biobank	rs1064796074
1000 genomes	rs1064796074
hgdp	rs1064796074
ensembl	rs1064796074
geneview	rs1064796074
scholar	rs1064796074
google	rs1064796074
pharmgkb	rs1064796074
gwascentral	rs1064796074
openSNP	rs1064796074
23andMe	rs1064796074
SNPshot	rs1064796074
SNPdbe	rs1064796074
MSV3d	rs1064796074
GWAS Ctlg	rs1064796074

Max Magnitude

0

ClinVar
Risk	rs1064796074(-;-)
Alt	rs1064796074(-;-)
Reference	Rs1064796074(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.97912296delG
CLNSRC
CLNACC	RCV000483255.1,