rs587783028

Orientation

minus

Stabilized

minus

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

Make rs587783028(G;T)

Make rs587783028(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

89752137

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs587783028
dbSNP (classic)	rs587783028
ClinGen	rs587783028
ebi	rs587783028
HLI	rs587783028
Exac	rs587783028
Gnomad	rs587783028
Varsome	rs587783028
LitVar	rs587783028
Map	rs587783028
PheGenI	rs587783028
Biobank	rs587783028
1000 genomes	rs587783028
hgdp	rs587783028
ensembl	rs587783028
geneview	rs587783028
scholar	rs587783028
google	rs587783028
pharmgkb	rs587783028
gwascentral	rs587783028
openSNP	rs587783028
23andMe	rs587783028
SNPshot	rs587783028
SNPdbe	rs587783028
MSV3d	rs587783028
GWAS Ctlg	rs587783028

Max Magnitude

0

ClinVar
Risk	rs587783028(A;A) rs587783028(T;T)
Alt	rs587783028(A;A) rs587783028(T;T)
Reference	Rs587783028(G;G)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCA
CLNDBN	Fanconi anemia, complementation group A
Reversed	1
HGVS	NC_000016.9:g.89818545C>A
CLNSRC
CLNACC	RCV000144483.1,