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Variant (rsID / SNP)

rs57268417

CRYBG2

rs57268417 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBG2. Location: chromosome 1, position 26,671,248. The table records no clinical significance for this variant.

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Reference-table entries

CRYBG2Not classified
Variant type
missense_variant
Chromosome / position
1:26671248
HGVS
NM_001039775.4,c.1901T>C,p.Val634Ala
Allele change
Missense_V634A

Public references

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