Variant (rsID / SNP)

rs11544446

rs11544446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBG3. Location: chromosome 3, position 97,660,084. The table records no clinical significance for this variant.

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Reference-table entries

CRYBG3Not classified

Variant type: synonymous_variant
Chromosome / position: 3:97660084
HGVS: NM_153605.4,c.8598C>T,p.Cys2866Cys
Allele change: Synonymous_C2866C

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.