Variant (rsID / SNP)

rs2960999

rs2960999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYW1B. Location: chromosome 7, position 72,193,868. The table records no clinical significance for this variant.

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Reference-table entries

TYW1BNot classified

Variant type: missense_variant
Chromosome / position: 7:72193868
HGVS: NM_001145440.3,c.1114C>T,p.Arg372Trp
Allele change: Missense_R372W

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.