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rs774506925

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs774506925(A;T)
Make rs774506925(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position101786206
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs774506925
ebirs774506925
HLIrs774506925
Exacrs774506925
Varsomers774506925
Maprs774506925
PheGenIrs774506925
hapmaprs774506925
1000 genomesrs774506925
hgdprs774506925
ensemblrs774506925
gopubmedrs774506925
geneviewrs774506925
scholarrs774506925
googlers774506925
pharmgkbrs774506925
gwascentralrs774506925
openSNPrs774506925
23andMers774506925
23andMe allrs774506925
SNP Nexus

SNPshotrs774506925
SNPdbers774506925
MSV3drs774506925
GWAS Ctlgrs774506925
Max Magnitude0
ClinVar
Risk rs774506925(T;T)
Alt rs774506925(T;T)
Reference rs774506925(A;A)
Significance Pathogenic
Disease I cell disease
Variation info
Gene GNPTAB
CLNDBN I cell disease
Reversed 0
HGVS NC_000012.11:g.102179984A>T
CLNSRC
CLNACC RCV000178995.1,