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SNP
ks616734245

Organism
Homo sapiens
Study
kstd16
RS ID
rs192947325
Submitted date
2026-05-13
Molecular Type
Genomic
Publication
Unpublished
Method Type
Sequencing
Variant Type
SNV
Sample Size
1
Position
chr2:225279513
Population
Korean
Alleles
G > C
Frequency
0.0151515

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

Genomic Placement
Sequence name Change
GRCh38
chr2
chr2.
225279513
G > C