rs878853663

Orientation

minus

Stabilized

minus

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

Make rs878853663(-;-)

Make rs878853663(-;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

89764937

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs878853663
dbSNP (classic)	rs878853663
ClinGen	rs878853663
ebi	rs878853663
HLI	rs878853663
Exac	rs878853663
Gnomad	rs878853663
Varsome	rs878853663
LitVar	rs878853663
Map	rs878853663
PheGenI	rs878853663
Biobank	rs878853663
1000 genomes	rs878853663
hgdp	rs878853663
ensembl	rs878853663
geneview	rs878853663
scholar	rs878853663
google	rs878853663
pharmgkb	rs878853663
gwascentral	rs878853663
openSNP	rs878853663
23andMe	rs878853663
SNPshot	rs878853663
SNPdbe	rs878853663
MSV3d	rs878853663
GWAS Ctlg	rs878853663

Max Magnitude

0

ClinVar
Risk	rs878853663(-;-)
Alt	rs878853663(-;-)
Reference	Rs878853663(CT;CT)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCA
CLNDBN	Fanconi anemia
Reversed	1
HGVS	NC_000016.9:g.89831345_89831346delAG
CLNSRC
CLNACC	RCV000231136.2,