rs781542763

Orientation

plus

Stabilized

plus

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

Make rs781542763(A;A)

Make rs781542763(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95171080

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs781542763
dbSNP (classic)	rs781542763
ClinGen	rs781542763
ebi	rs781542763
HLI	rs781542763
Exac	rs781542763
Gnomad	rs781542763
Varsome	rs781542763
LitVar	rs781542763
Map	rs781542763
PheGenI	rs781542763
Biobank	rs781542763
1000 genomes	rs781542763
hgdp	rs781542763
ensembl	rs781542763
geneview	rs781542763
scholar	rs781542763
google	rs781542763
pharmgkb	rs781542763
gwascentral	rs781542763
openSNP	rs781542763
23andMe	rs781542763
SNPshot	rs781542763
SNPdbe	rs781542763
MSV3d	rs781542763
GWAS Ctlg	rs781542763

Max Magnitude

0

ClinVar
Risk	rs781542763(A;A)
Alt	rs781542763(A;A)
Reference	Rs781542763(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	0
HGVS	NC_000009.11:g.97933362G>A
CLNSRC
CLNACC	RCV000169411.1,