rs527236197

Merged into

rs193303002

Orientation

plus

Stabilized

plus

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

Make rs527236197(A;A)

Make rs527236197(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15927

is a	snp
is	mentioned by
dbSNP	rs527236197
dbSNP (classic)	rs527236197
ClinGen	rs527236197
ebi	rs527236197
HLI	rs527236197
Exac	rs527236197
Gnomad	rs527236197
Varsome	rs527236197
LitVar	rs527236197
Map	rs527236197
PheGenI	rs527236197
Biobank	rs527236197
1000 genomes	rs527236197
hgdp	rs527236197
ensembl	rs527236197
geneview	rs527236197
scholar	rs527236197
google	rs527236197
pharmgkb	rs527236197
gwascentral	rs527236197
openSNP	rs527236197
23andMe	rs527236197
SNPshot	rs527236197
SNPdbe	rs527236197
MSV3d	rs527236197
GWAS Ctlg	rs527236197

Status

Merged into rs193303002

Max Magnitude

0

ClinVar
Risk	rs527236197(A;A)
Alt	rs527236197(A;A)
Reference	Rs527236197(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_012920.1:m.15927G>A
CLNSRC
CLNACC	RCV000133441.1,