rs561425038

Orientation

plus

Stabilized

plus

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

Make rs561425038(C;C)

Make rs561425038(C;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

35119613

Gene	FNDC8, RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs561425038
dbSNP (classic)	rs561425038
ClinGen	rs561425038
ebi	rs561425038
HLI	rs561425038
Exac	rs561425038
Gnomad	rs561425038
Varsome	rs561425038
LitVar	rs561425038
Map	rs561425038
PheGenI	rs561425038
Biobank	rs561425038
1000 genomes	rs561425038
hgdp	rs561425038
ensembl	rs561425038
geneview	rs561425038
scholar	rs561425038
google	rs561425038
pharmgkb	rs561425038
gwascentral	rs561425038
openSNP	rs561425038
23andMe	rs561425038
SNPshot	rs561425038
SNPdbe	rs561425038
MSV3d	rs561425038
GWAS Ctlg	rs561425038

Max Magnitude

0

ClinVar
Risk	rs561425038(A;A) rs561425038(C;C)
Alt	rs561425038(A;A) rs561425038(C;C)
Reference	Rs561425038(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RAD51D FNDC8 RAD51L3-RFFL
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.33446632T>A
CLNSRC	ClinVar GeneDx
CLNACC	RCV000484387.1,