rs730881708

Orientation

minus

Stabilized

minus

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

Make rs730881708(-;-)

Make rs730881708(-;GAGA)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95171110

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs730881708
dbSNP (classic)	rs730881708
ClinGen	rs730881708
ebi	rs730881708
HLI	rs730881708
Exac	rs730881708
Gnomad	rs730881708
Varsome	rs730881708
LitVar	rs730881708
Map	rs730881708
PheGenI	rs730881708
Biobank	rs730881708
1000 genomes	rs730881708
hgdp	rs730881708
ensembl	rs730881708
geneview	rs730881708
scholar	rs730881708
google	rs730881708
pharmgkb	rs730881708
gwascentral	rs730881708
openSNP	rs730881708
23andMe	rs730881708
SNPshot	rs730881708
SNPdbe	rs730881708
MSV3d	rs730881708
GWAS Ctlg	rs730881708

Max Magnitude

0

ClinVar
Risk	rs730881708(-;-)
Alt	rs730881708(-;-)
Reference	Rs730881708(GAGA;GAGA)
Significance	Pathogenic
Disease	not provided Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	not provided Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97933392_97933395delTCTC
CLNSRC
CLNACC	RCV000160466.2, RCV000410607.1,