rs875989813

Orientation

plus

Stabilized

plus

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

Make rs875989813(-;-)

Make rs875989813(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

45159081

Gene

FANCM

is a	snp
is	mentioned by
dbSNP	rs875989813
dbSNP (classic)	rs875989813
ClinGen	rs875989813
ebi	rs875989813
HLI	rs875989813
Exac	rs875989813
Gnomad	rs875989813
Varsome	rs875989813
LitVar	rs875989813
Map	rs875989813
PheGenI	rs875989813
Biobank	rs875989813
1000 genomes	rs875989813
hgdp	rs875989813
ensembl	rs875989813
geneview	rs875989813
scholar	rs875989813
google	rs875989813
pharmgkb	rs875989813
gwascentral	rs875989813
openSNP	rs875989813
23andMe	rs875989813
SNPshot	rs875989813
SNPdbe	rs875989813
MSV3d	rs875989813
GWAS Ctlg	rs875989813

Max Magnitude

0

ClinVar
Risk	rs875989813(-;-)
Alt	rs875989813(-;-)
Reference	Rs875989813(T;T)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	FANCM
CLNDBN	not specified
Reversed	0
HGVS	NC_000014.8:g.45628284delT
CLNSRC
CLNACC	RCV000171476.2,