rs149277003

Orientation

plus

Stabilized

plus

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

Make rs149277003(C;C)

Make rs149277003(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

89746890

Gene

FANCA

is a	snp
is	mentioned by
dbSNP	rs149277003
dbSNP (classic)	rs149277003
ClinGen	rs149277003
ebi	rs149277003
HLI	rs149277003
Exac	rs149277003
Gnomad	rs149277003
Varsome	rs149277003
LitVar	rs149277003
Map	rs149277003
PheGenI	rs149277003
Biobank	rs149277003
1000 genomes	rs149277003
hgdp	rs149277003
ensembl	rs149277003
geneview	rs149277003
scholar	rs149277003
google	rs149277003
pharmgkb	rs149277003
gwascentral	rs149277003
openSNP	rs149277003
23andMe	rs149277003
SNPshot	rs149277003
SNPdbe	rs149277003
MSV3d	rs149277003
GWAS Ctlg	rs149277003

Max Magnitude

0

ClinVar
Risk	rs149277003(C;C)
Alt	rs149277003(C;C)
Reference	Rs149277003(T;T)
Significance	Pathogenic
Disease	Fanconi anemia not provided
Variation	info
Gene	FANCA
CLNDBN	Fanconi anemia not provided
Reversed	0
HGVS	NC_000016.9:g.89813298T>C
CLNSRC
CLNACC	RCV000206698.3, RCV000254722.1,