rs794726667

Orientation

minus

Stabilized

minus

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

Make rs794726667(-;A)

Make rs794726667(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

95101828

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs794726667
dbSNP (classic)	rs794726667
ClinGen	rs794726667
ebi	rs794726667
HLI	rs794726667
Exac	rs794726667
Gnomad	rs794726667
Varsome	rs794726667
LitVar	rs794726667
Map	rs794726667
PheGenI	rs794726667
Biobank	rs794726667
1000 genomes	rs794726667
hgdp	rs794726667
ensembl	rs794726667
geneview	rs794726667
scholar	rs794726667
google	rs794726667
pharmgkb	rs794726667
gwascentral	rs794726667
openSNP	rs794726667
23andMe	rs794726667
SNPshot	rs794726667
SNPdbe	rs794726667
MSV3d	rs794726667
GWAS Ctlg	rs794726667

Max Magnitude

0

ClinVar
Risk	rs794726667(A;A)
Alt	rs794726667(A;A)
Reference	Rs794726667(-;-)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97864111dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012828.3,