rs587779904

Orientation

minus

Stabilized

minus

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

Make rs587779904(A;A)

Make rs587779904(A;TCTCAT)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95172133

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs587779904
dbSNP (classic)	rs587779904
ClinGen	rs587779904
ebi	rs587779904
HLI	rs587779904
Exac	rs587779904
Gnomad	rs587779904
Varsome	rs587779904
LitVar	rs587779904
Map	rs587779904
PheGenI	rs587779904
Biobank	rs587779904
1000 genomes	rs587779904
hgdp	rs587779904
ensembl	rs587779904
geneview	rs587779904
scholar	rs587779904
google	rs587779904
pharmgkb	rs587779904
gwascentral	rs587779904
openSNP	rs587779904
23andMe	rs587779904
SNPshot	rs587779904
SNPdbe	rs587779904
MSV3d	rs587779904
GWAS Ctlg	rs587779904

Max Magnitude

0

ClinVar
Risk	rs587779904(A;A)
Alt	rs587779904(A;A)
Reference	Rs587779904(TCTCAT;TCTCAT)
Significance	Pathogenic
Disease	not provided Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	not provided Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.97934415_97934420delATGAGAinsT
CLNSRC
CLNACC	RCV000115350.3, RCV000229758.2,