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SNP
ks616733239

Organism
Homo sapiens
Study
kstd16
RS ID
rs1559687178
Submitted date
2026-05-13
Molecular Type
Genomic
Publication
Unpublished
Method Type
Sequencing
Variant Type
SNV
Sample Size
1
Position
chr2:224894799
Population
Korean
Alleles
C > T
Frequency
0.0153846

Genomic regions, transcriptions, and products
Cytoband
Scale
Ref.hg38
RefSeqGene
GENCODE
KVAR

Genomic Placement
Sequence name Change
GRCh38
chr2
chr2.
224894799
C > T