rs797045116

Orientation

plus

Stabilized

plus

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

Make rs797045116(-;A)

Make rs797045116(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

45159190

Gene

FANCM

is a	snp
is	mentioned by
dbSNP	rs797045116
dbSNP (classic)	rs797045116
ClinGen	rs797045116
ebi	rs797045116
HLI	rs797045116
Exac	rs797045116
Gnomad	rs797045116
Varsome	rs797045116
LitVar	rs797045116
Map	rs797045116
PheGenI	rs797045116
Biobank	rs797045116
1000 genomes	rs797045116
hgdp	rs797045116
ensembl	rs797045116
geneview	rs797045116
scholar	rs797045116
google	rs797045116
pharmgkb	rs797045116
gwascentral	rs797045116
openSNP	rs797045116
23andMe	rs797045116
SNPshot	rs797045116
SNPdbe	rs797045116
MSV3d	rs797045116
GWAS Ctlg	rs797045116

Merged from

Rs761250416

Max Magnitude

0

ClinVar
Risk	rs797045116(A;A)
Alt	rs797045116(A;A)
Reference	Rs797045116(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCM
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.45628393dupA
CLNSRC
CLNACC	RCV000190644.1,