rs1060499606

Orientation

minus

Stabilized

minus

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

Make rs1060499606(-;-)

Make rs1060499606(-;CTCAT)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95172133

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1060499606
dbSNP (classic)	rs1060499606
ClinGen	rs1060499606
ebi	rs1060499606
HLI	rs1060499606
Exac	rs1060499606
Gnomad	rs1060499606
Varsome	rs1060499606
LitVar	rs1060499606
Map	rs1060499606
PheGenI	rs1060499606
Biobank	rs1060499606
1000 genomes	rs1060499606
hgdp	rs1060499606
ensembl	rs1060499606
geneview	rs1060499606
scholar	rs1060499606
google	rs1060499606
pharmgkb	rs1060499606
gwascentral	rs1060499606
openSNP	rs1060499606
23andMe	rs1060499606
SNPshot	rs1060499606
SNPdbe	rs1060499606
MSV3d	rs1060499606
GWAS Ctlg	rs1060499606

Max Magnitude

0

ClinVar
Risk	rs1060499606(-;-)
Alt	rs1060499606(-;-)
Reference	Rs1060499606(CTCAT;CTCAT)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.97934415_97934419delATGAG
CLNSRC
CLNACC	RCV000477851.1,