rs869312805

Orientation

plus

Stabilized

plus

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

Make rs869312805(-;-)

Make rs869312805(-;CCT)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10064804

Gene

FANCD2

is a	snp
is	mentioned by
dbSNP	rs869312805
dbSNP (classic)	rs869312805
ClinGen	rs869312805
ebi	rs869312805
HLI	rs869312805
Exac	rs869312805
Gnomad	rs869312805
Varsome	rs869312805
LitVar	rs869312805
Map	rs869312805
PheGenI	rs869312805
Biobank	rs869312805
1000 genomes	rs869312805
hgdp	rs869312805
ensembl	rs869312805
geneview	rs869312805
scholar	rs869312805
google	rs869312805
pharmgkb	rs869312805
gwascentral	rs869312805
openSNP	rs869312805
23andMe	rs869312805
SNPshot	rs869312805
SNPdbe	rs869312805
MSV3d	rs869312805
GWAS Ctlg	rs869312805

Max Magnitude

0

ClinVar
Risk	rs869312805(-;-)
Alt	rs869312805(-;-)
Reference	Rs869312805(CCT;CCT)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCD2
CLNDBN	Fanconi anemia, complementation group D2
Reversed	0
HGVS	NC_000003.11:g.10106488_10106490delCCT
CLNSRC
CLNACC	RCV000210268.1,