rs766105286

Orientation

plus

Stabilized

plus

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

Make rs766105286(A;A)

Make rs766105286(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

95111502

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs766105286
dbSNP (classic)	rs766105286
ClinGen	rs766105286
ebi	rs766105286
HLI	rs766105286
Exac	rs766105286
Gnomad	rs766105286
Varsome	rs766105286
LitVar	rs766105286
Map	rs766105286
PheGenI	rs766105286
Biobank	rs766105286
1000 genomes	rs766105286
hgdp	rs766105286
ensembl	rs766105286
geneview	rs766105286
scholar	rs766105286
google	rs766105286
pharmgkb	rs766105286
gwascentral	rs766105286
openSNP	rs766105286
23andMe	rs766105286
SNPshot	rs766105286
SNPdbe	rs766105286
MSV3d	rs766105286
GWAS Ctlg	rs766105286

Max Magnitude

0

ClinVar
Risk	rs766105286(A;A) rs766105286(T;T)
Alt	rs766105286(A;A) rs766105286(T;T)
Reference	Rs766105286(G;G)
Significance	Pathogenic
Disease	Fanconi anemia not specified Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia not specified Fanconi anemia, complementation group C
Reversed	0
HGVS	NC_000009.11:g.97873784G>A; NC_000009.11:g.97873784G>T
CLNSRC
CLNACC	RCV000206783.1, RCV000429828.1, RCV000205214.1, RCV000409033.1,