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SNP
ks620570612

Organism
Homo sapiens
Study
kstd16
RS ID
rs766732137
Submitted date
2026-05-13
Molecular Type
Genomic
Publication
Unpublished
Method Type
Sequencing
Variant Type
SNV
Sample Size
1
Position
chr16:63108338
Population
Korean
Alleles
C > A
Frequency
0.0230769

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

Genomic Placement
Sequence name Change
GRCh38
chr16
chr16.
63108338
C > A