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Variant (rsID / SNP)

rs10751735

CRYBG2

rs10751735 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBG2. Location: chromosome 1, position 26,663,362. The table records no clinical significance for this variant.

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Reference-table entries

CRYBG2Not classified
Variant type
missense_variant
Chromosome / position
1:26663362
HGVS
NM_001039775.4,c.3881G>A,p.Ser1294Asn
Allele change
Missense_S1294N

Public references

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