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Variant (rsID / SNP)

rs1159148

CRYBG1

rs1159148 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRYBG1. Location: chromosome 6, position 106,967,185. The table records no clinical significance for this variant.

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Reference-table entries

CRYBG1Not classified
Variant type
missense_variant
Chromosome / position
6:106967185
HGVS
NM_001371242.2,c.2102A>C,p.Gln701Pro
Allele change
Missense_Q293P

Public references

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