Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs63751103(-;-)
Make rs63751103(-;GGCAACCCTAAG)
Make rs63751103(GGCAACCCTAAG;GGCAACCCTAAG)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226712
GeneHBB
is asnp
is mentioned by
dbSNPrs63751103
ebirs63751103
HLIrs63751103
Exacrs63751103
Varsomers63751103
Maprs63751103
PheGenIrs63751103
hapmaprs63751103
1000 genomesrs63751103
hgdprs63751103
ensemblrs63751103
gopubmedrs63751103
geneviewrs63751103
scholarrs63751103
googlers63751103
pharmgkbrs63751103
gwascentralrs63751103
openSNPrs63751103
23andMers63751103
23andMe allrs63751103
SNP Nexus

SNPshotrs63751103
SNPdbers63751103
MSV3drs63751103
GWAS Ctlgrs63751103
Max Magnitude0
OMIM141900
Desc
Variant0284
Relatedalso
ClinVar
Risk rs63751103(GGCAACCCTAAGG,G;GGCAACCCTAAGG,G)
Alt rs63751103(GGCAACCCTAAGG,G;GGCAACCCTAAGG,G)
Reference rs63751103(GCAACCCTAAGG;GCAACCCTAAGG)
Significance Other
Disease HEMOGLOBIN TOCHIGI
Variation info
Gene HBB
CLNDBN HEMOGLOBIN TOCHIGI
Reversed 1
HGVS NC_000011.9:g.5247942_5247953delCTTAGGGTTGCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000016626.2,