rs730881731

Orientation

minus

Stabilized

minus

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

Make rs730881731(C;T)

Make rs730881731(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95240675

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs730881731
dbSNP (classic)	rs730881731
ClinGen	rs730881731
ebi	rs730881731
HLI	rs730881731
Exac	rs730881731
Gnomad	rs730881731
Varsome	rs730881731
LitVar	rs730881731
Map	rs730881731
PheGenI	rs730881731
Biobank	rs730881731
1000 genomes	rs730881731
hgdp	rs730881731
ensembl	rs730881731
geneview	rs730881731
scholar	rs730881731
google	rs730881731
pharmgkb	rs730881731
gwascentral	rs730881731
openSNP	rs730881731
23andMe	rs730881731
SNPshot	rs730881731
SNPdbe	rs730881731
MSV3d	rs730881731
GWAS Ctlg	rs730881731

Max Magnitude

0

ClinVar
Risk	rs730881731(T;T)
Alt	rs730881731(T;T)
Reference	Rs730881731(C;C)
Significance	Pathogenic
Disease	not provided Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	not provided Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.98002957G>A
CLNSRC
CLNACC	RCV000160499.1, RCV000472455.1,