rs876658297

Orientation

minus

Stabilized

minus

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

Make rs876658297(-;-)

Make rs876658297(-;TATG)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

35107108

Gene	RAD51D, RAD51L3-RFFL

is a	snp
is	mentioned by
dbSNP	rs876658297
dbSNP (classic)	rs876658297
ClinGen	rs876658297
ebi	rs876658297
HLI	rs876658297
Exac	rs876658297
Gnomad	rs876658297
Varsome	rs876658297
LitVar	rs876658297
Map	rs876658297
PheGenI	rs876658297
Biobank	rs876658297
1000 genomes	rs876658297
hgdp	rs876658297
ensembl	rs876658297
geneview	rs876658297
scholar	rs876658297
google	rs876658297
pharmgkb	rs876658297
gwascentral	rs876658297
openSNP	rs876658297
23andMe	rs876658297
SNPshot	rs876658297
SNPdbe	rs876658297
MSV3d	rs876658297
GWAS Ctlg	rs876658297

Max Magnitude

0

ClinVar
Risk	rs876658297(-;-)
Alt	rs876658297(-;-)
Reference	Rs876658297(TATG;TATG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51D RAD51L3-RFFL
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.33434127_33434130delCATA
CLNSRC
CLNACC	RCV000221453.1,