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rs35211634

From SNPedia

Orientationplus
Stabilizedplus
Make rs35211634(C;C)
Make rs35211634(C;T)
Make rs35211634(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position59845386
GeneGIF
is asnp
is mentioned by
dbSNPrs35211634
ebirs35211634
HLIrs35211634
Exacrs35211634
Varsomers35211634
Maprs35211634
PheGenIrs35211634
hapmaprs35211634
1000 genomesrs35211634
hgdprs35211634
ensemblrs35211634
gopubmedrs35211634
geneviewrs35211634
scholarrs35211634
googlers35211634
pharmgkbrs35211634
gwascentralrs35211634
openSNPrs35211634
23andMers35211634
23andMe allrs35211634
SNP Nexus

SNPshotrs35211634
SNPdbers35211634
MSV3drs35211634
GWAS Ctlgrs35211634
GMAF0.08494
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM609342
Desc
Variant0001
Relatedalso


ClinVar
Risk rs35211634(C;C)
Alt rs35211634(C;C)
Reference rs35211634(T;T)
Significance Other
Disease Intrinsic factor deficiency
Variation info
Gene GIF
CLNDBN Intrinsic factor deficiency, congenital, susceptibility to
Reversed 0
HGVS NC_000011.9:g.59612859T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001812.2,



GET Evidence
GIF-Q23R
aa_change Gln23Arg
aa_change_short Q23R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0989031
summary