rs794726668

Orientation

minus

Stabilized

minus

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

Make rs794726668(G;T)

Make rs794726668(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

95249126

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs794726668
dbSNP (classic)	rs794726668
ClinGen	rs794726668
ebi	rs794726668
HLI	rs794726668
Exac	rs794726668
Gnomad	rs794726668
Varsome	rs794726668
LitVar	rs794726668
Map	rs794726668
PheGenI	rs794726668
Biobank	rs794726668
1000 genomes	rs794726668
hgdp	rs794726668
ensembl	rs794726668
geneview	rs794726668
scholar	rs794726668
google	rs794726668
pharmgkb	rs794726668
gwascentral	rs794726668
openSNP	rs794726668
23andMe	rs794726668
SNPshot	rs794726668
SNPdbe	rs794726668
MSV3d	rs794726668
GWAS Ctlg	rs794726668

Max Magnitude

0

ClinVar
Risk	rs794726668(T;T)
Alt	rs794726668(T;T)
Reference	Rs794726668(G;G)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.98011408C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012831.3,