rs730881709

Orientation

minus

Stabilized

minus

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

Make rs730881709(-;T)

Make rs730881709(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95111489

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs730881709
dbSNP (classic)	rs730881709
ClinGen	rs730881709
ebi	rs730881709
HLI	rs730881709
Exac	rs730881709
Gnomad	rs730881709
Varsome	rs730881709
LitVar	rs730881709
Map	rs730881709
PheGenI	rs730881709
Biobank	rs730881709
1000 genomes	rs730881709
hgdp	rs730881709
ensembl	rs730881709
geneview	rs730881709
scholar	rs730881709
google	rs730881709
pharmgkb	rs730881709
gwascentral	rs730881709
openSNP	rs730881709
23andMe	rs730881709
SNPshot	rs730881709
SNPdbe	rs730881709
MSV3d	rs730881709
GWAS Ctlg	rs730881709

Max Magnitude

0

ClinVar
Risk	rs730881709(T;T)
Alt	rs730881709(T;T)
Reference	Rs730881709(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.97873772dupA
CLNSRC
CLNACC	RCV000160468.1, RCV000203768.2,