rs753885687

Orientation

plus

Stabilized

plus

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

Make rs753885687(C;G)

Make rs753885687(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95107065

Gene	C9orf3, FANCC, LOC107987102

is a	snp
is	mentioned by
dbSNP	rs753885687
dbSNP (classic)	rs753885687
ClinGen	rs753885687
ebi	rs753885687
HLI	rs753885687
Exac	rs753885687
Gnomad	rs753885687
Varsome	rs753885687
LitVar	rs753885687
Map	rs753885687
PheGenI	rs753885687
Biobank	rs753885687
1000 genomes	rs753885687
hgdp	rs753885687
ensembl	rs753885687
geneview	rs753885687
scholar	rs753885687
google	rs753885687
pharmgkb	rs753885687
gwascentral	rs753885687
openSNP	rs753885687
23andMe	rs753885687
SNPshot	rs753885687
SNPdbe	rs753885687
MSV3d	rs753885687
GWAS Ctlg	rs753885687

Max Magnitude

0

ClinVar
Risk	rs753885687(G;G)
Alt	rs753885687(G;G)
Reference	Rs753885687(C;C)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	0
HGVS	NC_000009.11:g.97869347C>G
CLNSRC
CLNACC	RCV000409707.1,