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rs1057518337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518337(A;G)
Make rs1057518337(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position79042898
GenePHIP
is asnp
is mentioned by
dbSNPrs1057518337
dbSNP (old)rs1057518337
ClinGenrs1057518337
ebirs1057518337
HLIrs1057518337
Exacrs1057518337
Gnomadrs1057518337
Varsomers1057518337
LitVarrs1057518337
Maprs1057518337
PheGenIrs1057518337
Biobankrs1057518337
1000 genomesrs1057518337
hgdprs1057518337
ensemblrs1057518337
gopubmedrs1057518337
geneviewrs1057518337
scholarrs1057518337
googlers1057518337
pharmgkbrs1057518337
gwascentralrs1057518337
openSNPrs1057518337
23andMers1057518337
23andMe allrs1057518337
SNPshotrs1057518337
SNPdbers1057518337
MSV3drs1057518337
GWAS Ctlgrs1057518337
Max Magnitude0
ClinVar
Risk rs1057518337(G;G)
Alt rs1057518337(G;G)
Reference Rs1057518337(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHIP
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.79752615T>C
CLNSRC
CLNACC RCV000414004.1,