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Variant (rsID / SNP)

rs783396

CRYBG1

rs783396 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBG1. Location: chromosome 6, position 106,987,370. The table records no clinical significance for this variant.

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Reference-table entries

CRYBG1Not classified
Variant type
missense_variant
Chromosome / position
6:106987370
HGVS
NM_001371242.2,c.4811A>C,p.Glu1604Ala
Allele change
Missense_E1196A

Associated conditions / phenotypes

Stroke, Ischemic

Public references

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