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rs1057520162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520162(G;T)
Make rs1057520162(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position53637728
GeneRPGRIP1L
is asnp
is mentioned by
dbSNPrs1057520162
dbSNP (old)rs1057520162
ClinGenrs1057520162
ebirs1057520162
HLIrs1057520162
Exacrs1057520162
Gnomadrs1057520162
Varsomers1057520162
Maprs1057520162
PheGenIrs1057520162
Biobankrs1057520162
1000 genomesrs1057520162
hgdprs1057520162
ensemblrs1057520162
gopubmedrs1057520162
geneviewrs1057520162
scholarrs1057520162
googlers1057520162
pharmgkbrs1057520162
gwascentralrs1057520162
openSNPrs1057520162
23andMers1057520162
23andMe allrs1057520162
SNPshotrs1057520162
SNPdbers1057520162
MSV3drs1057520162
GWAS Ctlgrs1057520162
Max Magnitude0
ClinVar
Risk rs1057520162(T;T)
Alt rs1057520162(T;T)
Reference Rs1057520162(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGRIP1L
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.53671640C>A
CLNSRC
CLNACC RCV000425777.1,