rs137852864

Orientation

plus

Stabilized

plus

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

Make rs137852864(A;A)

Make rs137852864(A;C)

Reference

GRCh38 38.1/141

Chromosome

14

Position

45173065

Gene

FANCM

is a	snp
is	mentioned by
dbSNP	rs137852864
dbSNP (classic)	rs137852864
ClinGen	rs137852864
ebi	rs137852864
HLI	rs137852864
Exac	rs137852864
Gnomad	rs137852864
Varsome	rs137852864
LitVar	rs137852864
Map	rs137852864
PheGenI	rs137852864
Biobank	rs137852864
1000 genomes	rs137852864
hgdp	rs137852864
ensembl	rs137852864
geneview	rs137852864
scholar	rs137852864
google	rs137852864
pharmgkb	rs137852864
gwascentral	rs137852864
openSNP	rs137852864
23andMe	rs137852864
SNPshot	rs137852864
SNPdbe	rs137852864
MSV3d	rs137852864
GWAS Ctlg	rs137852864

Max Magnitude

0

OMIM	609644
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137852864(A;A)
Alt	rs137852864(A;A)
Reference	Rs137852864(C;C)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCM
CLNDBN	Fanconi anemia, complementation group M
Reversed	0
HGVS	NC_000014.8:g.45642268C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001665.4,