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rs7297245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(T;T) 0 common on affy axiom data
Make rs7297245(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position95980836
GeneHAL
is asnp
is mentioned by
dbSNPrs7297245
dbSNP (classic)rs7297245
ClinGenrs7297245
ebirs7297245
HLIrs7297245
Exacrs7297245
Gnomadrs7297245
Varsomers7297245
LitVarrs7297245
Maprs7297245
PheGenIrs7297245
Biobankrs7297245
1000 genomesrs7297245
hgdprs7297245
ensemblrs7297245
geneviewrs7297245
scholarrs7297245
googlers7297245
pharmgkbrs7297245
gwascentralrs7297245
openSNPrs7297245
23andMers7297245
SNPshotrs7297245
SNPdbers7297245
MSV3drs7297245
GWAS Ctlgrs7297245
GMAF0.1093
Max Magnitude0
? (C;C) (C;T) (T;T) 28




[PMID 18641401OA-icon.png] A role for ultraviolet radiation immunosuppression in non-melanoma skin cancer as evidenced by gene-environment interactions.


[PMID 18853455OA-icon.png] Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.



ClinVar
Risk Rs7297245(T;T)
Alt Rs7297245(T;T)
Reference Rs7297245(C;C)
Significance Non-pathogenic
Disease Histidinemia
Variation info
Gene HAL
CLNDBN Histidinemia
Reversed 0
HGVS NC_000012.11:g.96374614C>T
CLNSRC
CLNACC RCV000385709.1,